© Distribution of this video is restricted by its owner
Transcript ×
Auto highlight
Font-size
00:01 Yeah. Ok. Ok, Uh, let's get started here.

00:30 , 14, uh, we only a couple of flights left on

00:35 So, um, then 16, 16, 17 immune system.

00:43 It's gonna start the immune system, , in a few minutes.

00:48 uh, that will go on to week and then, uh, on

00:53 17. So, uh, see back to weekly quizzes, um,

01:00 , uh, so just be aware that coming up due on Monday.

01:05 , uh, let's see. exam two was opened up yesterday.

01:10 I forgot to, like I mentioned in today's email. So,

01:13 do take a look at it if got questions. Uh, let me

01:17 , but give yourself a chance to through it. See if you can

01:20 through the questions, few minutes, if you can figure it out.

01:23 not, I'll, I'll certainly let , uh, let me know.

01:27 . Uh, let's see what So, uh, our exams not

01:32 another three weeks yet, but uh, scheduler for that will open

01:38 Friday for that exam. Ok. , um, anyway, uh,

01:45 approaching the end here. Ok. let's, uh, look at.

01:55 again, as I mentioned several times , 14 is a lot of

02:00 right? So you've got a um list here. I just, I

02:06 literally just went through the slides and , just put them and group them

02:09 together. OK. So, uh why this is really just writing these

02:15 out and just remembering them? Um So the uh uh last

02:24 OK, we talked about uh the last very last thing we talked

02:29 was epidemiology, right? So that's um data, you know, basically

02:35 at data uh which are um data instance, instances of disease. Um

02:45 looking at it in different ways uh it to, to um maybe find

02:52 cause of a disease to find out you can prevent disease. Um try

02:58 use it to, to um figure what's the source of the illness?

03:03 Is there a particular demographic group that's susceptible to it? So, lots

03:08 different ways to use the data. And these are some examples here,

03:12 three ways. So what they describe um descriptive, analytical and um uh

03:21 the other one, other name, other one is called uh experimental.

03:27 . And grand there is some overlap these because they're all looking at

03:31 OK? All three of course but in um descriptive epidemiology, I

03:36 realized uh Jon Snow, anybody if know who Jon Snow is Game of

03:43 I feel like, so that's not Jon Snow, obviously, although they're

03:47 British, I guess. Uh, , but anyway, mm,

03:53 um, so he used, this , and his study was kind of

03:57 the fact, uh, more or so cholera outbreak in London, which

04:02 a very common thing during that these , like mid 18 hundreds, I

04:06 , uh, people used the main going through London, that's kind of

04:09 water source for everything both to use dump into. Um And so water

04:15 be pumped there uh in various neighborhoods like a old fashioned you might be

04:20 of, you know, back, in these days, you know,

04:22 pumped water with one of these things out of a spout in the middle

04:26 a neighborhood and that's where people go their water. And so just by

04:30 around to these neighborhoods, he just looked at um death records of

04:35 People had died from cholera and then kind of went from house to house

04:41 asking, ok, who, who your family had it? Where were

04:45 at uh before they became sick, kind of things and they kind of

04:49 together a map of, of the um in downtown London and saw a

04:55 number of cases where the red arrow at and then it was traced to

04:58 , a particular pump and it had faulty uh contaminated or some something when

05:05 changed it out uh to a brand pump, the instances of cases went

05:11 down, but you wouldn't have known if, if you hadn't done this

05:14 of these studies. And so um what we call descriptive. And so

05:20 analytical is obviously looking at a ton statistical data, this is what Florence

05:26 did. Um looking at uh So typhus is a disease that is

05:35 um a disease of poor sanitary bad hygiene, um close quarters being

05:44 . Um It could be um you , it's carried by fleas, uh

05:51 types of fleas and ticks, Ok. Uh Many are carried by

05:56 , mice and rats and things. so, um it produces kind of

05:59 a fever and uh um headache and symptoms become worse after that. But

06:07 it was a common uh in this and before this time, it was

06:10 common because of course, didn't have sanitary conditions we do nowadays in most

06:15 . And so that contributed heavily to disease. But she was interested in

06:19 at, you know, what is nature of this compared to our

06:24 right? Looking at military members of military compared to just the average,

06:28 know, civilians. Ok. And is the difference in terms of

06:33 these cases of typhus? And so me just flip, flip forward real

06:37 just to show you. So he just looking at this is actually looking

06:40 both typhus and cholera, you they label it contagious diseases. But

06:46 was basically looking at both of these primarily typhus. So, cholera is

06:49 waterborne, you know, uh, contaminated water. And so,

06:54 of course, in the military, , they're, you know, they're

06:57 together, uh, at this you know, they may not have

07:01 best hygiene, uh, uh, not bathing regularly, stuff like

07:06 Um, she also e especially, know, for those that are just

07:11 that were in England, right? a higher than the, than the

07:14 public. Ok, 0.2 versus But then when you look at soldiers

07:19 in war, war time, in a, uh, I forget

07:24 Crimean War, uh, that it much higher. And so,

07:28 attributed to that, she attributed, saw, she investigated this and

07:32 ok, what's different here in this compared to these other two groups is

07:38 poor nutrition, right? So that , that's gonna lower your immune system

07:43 unsanitary conditions, uh, poor you know, poor, um,

07:48 day to day conditions overall. And all together contributing to, um,

07:52 , these higher instances of typhus. so when she saw this and

07:57 well, let's do Xy and Z minimize these things to get better

08:02 clean up, uh, bathe et cetera, et cetera. And

08:07 course, instances go way down to to 2%. Pretty significant.

08:13 And so apparently she, she had this 1000 page report with a bunch

08:17 tons of graphs and data and numbers things. Uh That's of course,

08:21 definitely fits it being an analytical um do you call analytical um epidemiology?

08:29 . The experimental, it is kind like uh basically setting up an

08:34 a control group and a and a experimental group in similar ways. I

08:39 have briefly talked about this earlier but back in the first chapter. But

08:46 he insti instituted the use of an antiseptics ansis. And so in the

08:53 , he was working at um he that uh the in the hospital,

09:01 the the ward where women went to give birth, that there was a

09:05 high incidence of this disease called child fever is kind of the layman's term

09:11 fever is the medical term. It's to uh streptococcus bacterium um acquired during

09:19 . Uh the baby uh can contract as well as it can spread into

09:24 uterus and then also affect the So both mother and baby can be

09:29 . Um And so he said, , what is, what's contributing to

09:33 ? Because he saw this group here the hospital that had a really high

09:37 of this disease. And then he um you know, women that didn't

09:43 to the hospital gave birth outside the or uh used a midwife that they

09:50 outside the hospital that they were, much lower instance of this. And

09:53 he looked and saw what's the common here. Well, uh, these

09:58 groups, um, washed their That was a regular practice of washing

10:03 as a woman is about to give . And in the hospital, the

10:08 , um, Maternity ward. no, um, where women were

10:13 birth, uh, the doctors that , that were the young doctors.

10:19 so they would be like 1st, year medical students that would come out

10:24 a um uh uh Cadaver ward. , of course, as a

10:29 you work on cadavers, you study the body and how it works

10:32 whatnot. They would come directly from to the maternity ward, of

10:36 dirty and bloody in hands and not and not depriving way. That's,

10:41 what contributed to the high instance of child had fever. And so when

10:45 instituted said you aren't going in there you wash your hands. And so

10:50 that, I mean, the numbers dropped much like the uh what we

10:54 with, uh, with, uh like a rate that's that like that

11:01 se drop just again, just washing hands, right. So,

11:06 but actually in, back in the it was uh a much harsher soap

11:10 . It was this Li Live which is actually very, almost like

11:14 your hands with bleach almost, So, uh that definitely is gonna

11:18 any bacteria and likely kill some of own cells on there. But uh

11:22 did definitely lead to this drop in number of diseases. OK. Of

11:26 particular one referring to uh child bed . So, um no, we

11:33 heard of uh clinical trials, you , when your drug is on the

11:36 , then you test different groups, ? Could be uh one who gets

11:40 placebo, one doesn't these kind of that all falls into the the uh

11:46 of experimental epidemiology. OK. So the case reporting, so I mentioned

11:55 already as well. So case reporting nationally notifiable diseases kind of goes hand

12:00 hand. OK. So there let me just quickly show do not

12:06 this table obviously, but um these the nasty notifiable diseases. Uh And

12:13 what you might think, you communicable diseases, obviously, things like

12:17 , mumps, uh et cetera, uh influenza COVID. Um And then

12:24 all of your sexually transmitted diseases fall this group. Uh and then certainly

12:28 number of others. OK. And with this data, of course,

12:33 you can um see if there's an is, is what's going on and

12:39 to break that chain of transmission, call it OK. To, to

12:44 to contain the disease. So uh information to have. So we can

12:50 and it's basically all that information is put together in this publication here

12:58 which covers every infectious disease, I even non infectious diseases too.

13:05 on a weekly basis, you they track all this data if they

13:08 something that's, you know, spiking or what have you, then they

13:12 on the course and, and, follow it to see if it become

13:16 significant. Um, and you, know, if you're interested, you

13:19 , we just Google that and you , you can see the actual weekly

13:23 here. The ones at the end the year are kind of interesting.

13:26 kind of overview of, of the year and the, and, and

13:30 has every infectious disease in the number cases that are during the year.

13:36 , but, uh, and so that, the, the terms,

13:39 you see morbidity and mortality. So, um, I'm sure you

13:46 heard of mortality, obviously. So rate, number of deaths,

13:49 It's about deaths from these diseases. , morbidity is, is the uh

13:55 or rather the instance of a specific . Ok. You don't necessarily die

13:59 it, but you report it people are reported to have it.

14:04 been confirmed from testing that they have disease, uh whether they fall into

14:09 mortality category, of course, depends they die from. Hi, this

14:27 number than mortality, mortality and morbidity . That's like 100% mortality rate.

14:35 ? You get the symptoms of disease you die, right? So you're

14:38 gonna be the same. Ok. , I mean, I guess it

14:44 be close if it was something like but even with that it's not,

14:48 not equal. So generally morbidity is be higher, right? You have

14:51 lot of people that come down with , right? Contributing to the morbidity

14:57 . But how many are gonna actually ? Right. Much less are gonna

15:00 than actually. Yeah. Does that sense? That morbidity is gonna be

15:05 mortality? How they relate? Um . So I see that that ends

15:15 . OK. Any questions about right? OK. So let's uh

15:22 we're going to innate community. So parts here, innate and adaptive,

15:26 community. 17. Uh and that is one of those uh uh you're

15:31 kind of work on it yourself, ? So the, I think the

15:35 should be available, the lecture video stuff. So go ahead and take

15:40 look at that stuff already for for 17. OK. And we'll

15:44 through that next Thursday. OK. I have a bunch of questions and

15:50 kind of frame it around that. again, you've seen this already 100

15:54 , but again, just to we're not gonna focus on this is

16:00 this really host offensive. OK. Which of course relates to, you

16:07 , do you come down with What's your level of resistance or you're

16:12 so resistant? You, are you susceptible? OK. Of course,

16:15 relates to your, your immune obviously. Ok. So with the

16:19 immune system, that's what you come of the, you know, come

16:25 , right? You're born and you've got that innate immune system already

16:29 , not, you know, as baby, obviously, not at the

16:32 level as it will a few months years from that point. But you

16:37 have, obviously skin, that's a barrier, certainly part of innate immune

16:41 . You have mucous membranes lining your cavities and whatnot. That's, that's

16:45 of it. Um We all we call the innate immune system,

16:52 . OK. And there's a reason that, but let's look first at

16:55 question here just to see if we uh uh come up with something

17:00 So I remember so as we go this, your, your innate and

17:05 immune system, you can look at as 12 and three in terms of

17:10 . And one way to visualize that really if you're a, if you're

17:14 pathogen out here, right? And comes into the body, OK?

17:19 are the layers that's going through, ? As it penetrates deeper into your

17:24 if it does. OK. And that's one way to look at it

17:27 terms of first line, second third line. OK. Um Let's

17:37 . Um So as you're answering so specific versus non-specific, so

17:44 the immune system is the adaptive immune . OK? Because it relies

17:50 on um binding of components to each antigen antibody very often. So there's

17:59 , there's a different specificity to it it involves a binding OK to an

18:04 . OK. And that's what sets motion. All the things that

18:09 OK. Your, your innate immune is not all, there is molecules

18:15 in certain in parts of the It's not all centered on that.

18:20 about microbes coming in and you have barriers that they can encounter and may

18:27 may not get through, but it's as specific as the adaptive immune

18:32 OK. So let's count down here 10. All right. Um

18:48 that's uh yeah, it, you're correct. It's fever, fever

18:52 , is I think more of a line defense. OK? And so

18:57 look at um both sides of this here. Here we go. So

19:04 non-specific and specific. OK. So system falls in that category,

19:11 Um And so first line, so I said, picture microbe here is

19:15 in, right? What's it gonna first skin skin barrier? Then if

19:20 like gets into your nose or maybe mucous membranes line your nasal

19:24 Um you ingest it, right? mucous membranes coat your throat and then

19:31 uh test. And so basically, a colleague of mine that teaches a

19:37 and human phys. Uh this gives analogy that the body is a

19:42 OK. It goes right through, through your mouth. Butt.

19:46 It's the whole, right exposed to environment, right? But they have

19:51 f around your guts and everything else it. So, of course,

19:55 what goes through the hole is what breathe in uh ingest. And of

20:01 , that will contain uh micros, they encounter, right, the mucus

20:06 as they pass through. So, so skin these membranes uh and don't

20:12 forget your, your own microbiome, ? They're, they're a part of

20:17 certainly as well. OK. Now gonna be uh somewhat redundant because um

20:25 your first line defense, you can at these especially um skin and mucus

20:35 um as a physical barrier. But they also produce a chemical

20:41 which means skin and mucus membranes produce and those chemicals also can interact

20:48 in uh counteract pathogens that come So, so your first line of

20:55 is both a chemical physical and chemical as, as you'll see um second

21:01 effect. So getting past your, um first line, then second line

21:08 kind of characterize as cells, specific that are meant to interact with pathogens

21:14 get rid of them and also So I call like inflammation,

21:20 these I call processes, these of are particular cell types right now,

21:27 the processes of course involve cells. ? But you one of your main

21:33 to find infection, of course is foc cytosis, literally just engulfing pathogens

21:39 , and breaking them up. I . So, uh so there's a

21:44 of a number of um cells and processes that are part of the second

21:48 of defense. And so the third , which we won't get to until

21:51 week, from the day is your immune system. So this requires um

21:58 , it only gets activated. So the respond two, that's what

22:10 that system, right? Um And uh it's, that's why we have

22:17 , that's what we call it So you have um cells in your

22:21 system that their immune system will recognize . Ok? Um Antibodies is one

22:30 production of antibodies. You can of the thousands, if not millions

22:34 potential engines out there, you can produce antibodies to each and every one

22:39 them allergies are about kind of a response to certain antigens. What in

23:06 case, the uh and so uh cells and B cells, I remember

23:16 also a couple of other types and also gonna see is that there will

23:22 cell types that will bridge that both . You have cell types that both

23:30 part of the adaptive and inane. they were kind of connected to.

23:38 um so ha knowing I just told now, let's uh see this is

23:46 , this is a and which responds , right? Ory and Nate.

23:56 I'm not going to run the timer this one all winding down. All

24:29 . Counting down from four. yes, it, they gonna be

24:39 they, and, and it really to do with that, that having

24:44 , well, the engine, the response or response to antigen, which

24:52 what the adaptive immune system relies Ok. Um, there are 22

25:00 . One is, um, ok. Identify, find it,

25:11 to speak. Ok. And then it. Uh It's gonna be

25:23 not scientific but uh I'll just say stuff. OK. I'll elaborate on

25:33 . Of course, it's uh a too bad but do stuff means

25:37 so uh identifying to recognizing and finding right? There is a time element

25:41 that doesn't happen instantaneously, right? Then you buy an engine and then

25:47 then induces a lot of stuff going inside the cell. Now making different

25:54 of molecules, et cetera, et . And then, um that,

25:59 then leads to so the new stuff then those antibodies leave or it so

26:04 finds the engine and then stuff right? More stuff happens. So

26:09 uh uh for now this is, is why you, we'll get the

26:13 and bolts uh next week. But um so yeah, it, this

26:18 takes time, right? So of , the, the Navy service is

26:21 there, right? It's, it's barrier, it stops or OK.

26:26 again, I put the kind of terms in this, uh,

26:31 chattered together here. Ok. So get, I broke it down in

26:36 of chemical defenses, physical barriers or the skin mucus membranes, right?

26:41 , different cell types we see Ok. Um, another cell type

26:48 that immune system relies on antigen. , this is another one, cytokines

26:54 something you'll hear over and over. . So these, it's basically a

27:00 term, chemicals that, um, tell other cells of the immune system

27:07 to do. Uh And they have variety of different functions as you'll

27:12 Um And names the cytokine is kind the generic name, but there are

27:17 names for all these things. Um then here are some uh processes here

27:23 this box. OK? Um PS . Not sure. You know what

27:29 is yet, we'll talk about Uh figy tosis. The other thing

27:35 uh the type of pathogen your body to deal with. OK. Will

27:43 two different strategies. OK? You're have pathogens who do their thing.

27:51 now this is in your body. ? Do their thing by being outside

27:55 , right? So what we call pathogen. OK. But then there

28:00 types that go inside your cells and their motive infection, right?

28:06 for example. Uh So you have in intercellular and intercellular pathogens, but

28:11 have to have two very different ways dealing with that. OK? Because

28:15 a pathogen is inside a cell, kind of hidden from the body.

28:21 . And so there has to be way to identify those kind of infected

28:26 and there is all right. so there's gonna be ways to deal

28:29 both. OK. So, you , rule of thumb typically is phagocytosis

28:36 work if it, if it's inside a cell. Right. Certainly,

28:41 it's outside, you can just something the foc cytosis engulf it and chew

28:44 up. Uh So we, we see there's different strategies for for what

28:50 of pathogen is and how we can be. And we used to call

29:08 lamps, lamps, PMS M AM . Yes. What it did.

30:29 so thank you positive, right? all of it. Um And

30:44 and also your book doesn't go into and I'm not gonna touch you on

30:47 , but cells have to receptors, have a bunch of cells in your

31:25 that have these um uh and, when they encounter a pathogen like

31:31 then that, that signal sort of a sets in the motion of production

31:41 cytokines. OK. As I you have a lot of different

31:45 OK? From you just a OK. I will mention these as

31:50 go through. But uh is the the with octopus with a bunch of

32:34 arms, right? That would be active but no arms, right?

32:42 an OK. You see the positive an infection somewhere is to get your

33:06 to that site. And so right? There's, there's movement toward

33:11 chemical. And so that's what that . OK. So if you have

33:16 skin cut or wound or something here whatever, these chemotactic signals will draw

33:24 immune system cells there. Uh inflammatory , fever, um that will go

33:30 that. Uh not today, but time. Uh so again, these

33:33 typical responses. We've all had we've all had inflammation, right?

33:38 are specific responses really. Uh inflammation really about um containing infectious agent where

33:49 entered the body, so to So if you have like a splinter

33:52 , and it's contaminated and you have infection that the inflammatory response is meant

33:57 kind of contain it right there and let it spread. Um, fever

34:04 its own use, ok? Um T and B cells. So that's

34:09 the adaptive. So again, these just four things, five things,

34:15 cytokines do a bunch of other stuff well. OK. But all,

34:20 kind of activating some part of the system. Ok. So back to

34:24 ? So think of this system on slide here, this total like receptor

34:31 , right? This is really it's, it's the the it's like

34:37 the um you smell smoke in a and you pull the fire to alert

34:43 . That's kind of what this The toilets are kind of to alert

34:47 body. Let's get uh let's get kind of thing. Ok. And

34:54 wouldn't do that and outside of kinds that will uh get certain cells to

35:00 as needed. Ok. So to receptors are kind of the alarm

35:06 So to like receptors themselves, these , right? These things do not

35:11 anything, right? They don't have role in killing a pathogen. Their

35:17 is in warning the body of a pathogen is present and let's get,

35:22 do something. OK. That's what is, right? Um So

35:28 it's probably obvious to you, but it's like the total receptor is not

35:33 cell, it's a protein on a surface that interacts with A P A

35:39 and that activates it. Yeah. OK. So first line defenses.

35:44 it's going to be a little bit , as I said. So we

35:46 at it first as a physical So skin of course, is a

35:51 uh thick layer of, of multiple of cells. OK. Epithelial

35:58 And so that in itself provides a barrier. But then you put in

36:04 kind of um protein material that kind holds it together and covers it.

36:08 rich in keratin. OK. Keratin very and it, it's on the

36:15 of your body, but it's very on your fingernails because that your fingernails

36:19 basically you hair. OK. But but your body is covered with this

36:25 is covered with this as well. it makes it very, almost i

36:29 Impenetrable but very stout barrier. But do have of course natural openings in

36:35 skin, right? You have uh , right? Um sweat glands,

36:40 hair follicles. So these are kind can be natural openings where bacteria may

36:44 able to enter. Ok. And course, you have a cut or

36:50 a way for bacteria to penetrate your through a wound. That's typically what

36:54 call subcutaneous infection. OK. So membranes of course line, which means

37:01 the G I tract, obviously gu respiratory tract, et cetera.

37:06 And they typically have a structure like uh a basement, we often call

37:12 basement membrane. Don't need to worry that term. But as the blue

37:17 of like the foundation and then on of that, you have various

37:21 this should be cells from your intestine cells are part of that. Um

37:26 so, but again, very very dense uh and often producing uh

37:33 I'll uh I'll just here, membranes some sort of a secretion as what's

37:38 mucus is a secretion right? To the cells moist uh in the intestine

37:44 serves also the function of a lot food pass through. Um but mucus

37:50 nature of it can also help track uh plus your, your um Celia

37:59 your throat formed this thing called the , you're a senior. Well,

38:22 40 of P and those hairs, stuff, right? Just like filia

39:11 your throat. Um, ch and . Uh, so you always have

39:18 eyes. Well, some are your , uh, but that, you

39:24 , tears are for that to kind keep washing eyes, wash micro out

39:29 , we wash over your teeth and . Um, so, and

39:36 and then as well, ear walking does have a function testing it

39:40 It may be, uh, the bugs in your ears, ok.

39:46 as well make insect anyway. Um uh and certainly a digestion,

39:52 You eliminate lots of pressure pass through system. Uh epiglottis, that's the

39:59 covers your windpipe, you fall. you don't get things in your

40:03 So yeah, all these are part that helping kind of prevent at least

40:08 best they can microbes from getting into , stopping them where they're at more

40:13 less. Ok. So again, of these or most of these will

40:17 act as chemical uh barriers. So, because they all have secretions

40:25 tends to be kind of a salty , acidic uh because of the kind

40:30 molecules that are produced there. And that in itself is a way to

40:34 of um uh affect what can actually there. Ok. Uh Staphylococcus likes

40:41 conditions, which is why Staph is of the main bacteria you have on

40:45 skin. Um Another one the mucus . So saliva gastric reduce obviously

40:52 very low ph um vaginal secretion is acidic, urine is also actually slightly

40:59 . But the one common thing in in many of these is I circled

41:04 here is Lysol, OK. In places right now, I can,

41:14 that material? That is what they long. OK. So uh so

41:21 a a defense against the bacterial types that have so long. And so

41:28 , as mentioned before, we talked this, that uh this is part

41:32 your immune system as well, your microbiota. So they're mere, they're

41:37 alone to keep other things from taking . Um And they, they produce

41:43 own kind of micro environments that can times prevent things from growing there.

41:49 very essential. Um OK. So line uh physical and chemical barriers,

41:58 after them, our second line. so we start with kind of different

42:03 types, uh specific cell types involved this. So you break down

42:08 so your plasma fracture, your um you have a protein fraction,

42:14 plasma that contains antibodies and complement and types of proteins. The um the

42:22 part of this contains what are called elements. So red blood cells,

42:25 blood cells um are basically are um of hemoglobin and hemoglobin binds oxygen.

42:38 . Uh Red blood cells don't have nucleus. OK. Um But uh

42:45 also are not really cells or fragments involve in clotting. Uh But the

42:50 types, of course, are your , your white blood cells um of

42:55 types. And so these, this of granulocytes and a granulocytes. Uh

43:02 little bit deceiving because um they they all can have Granules.

43:11 It's just that when you look at under a light microscope, it's much

43:16 obvious in these types. Neutrophils, , eosinophils, you look at it

43:20 go. Oh yeah, that's that's a granny appearance thing. We

43:23 lots of Granules. Ok? Um just not as visible under the microscope

43:28 these guys all, they all they have. Ok. But anyway,

43:32 , it's uh some type of It's uh it's a historical thing and

43:37 never changes, but that's, that's they still refer to them, the

43:40 sites and a granular sites. Um so we'll go through each of these

43:46 . Um All right, nut. neutral shows are gonna be your early

43:51 in infection is neutrophils that are your foc cytic cell types that do the

43:59 of the work initially, right? So neutrophils are in blood. So

44:04 see, there's 70% and don't worry much about these percentages. Uh but

44:10 just to show that they are, know, in the highest quantity of

44:13 blood. And so if they're in blood and you have an infectious agent

44:20 in your tissues outside the blood, , then you have to get them

44:25 of the blood into the surrounding Ok. And that's what neutrophils

44:29 Ok. So the eggs of it is all part of that inflammatory

44:35 which will work next time. But uh but you know, I pulling

44:43 everywhere in your body, they're in bloodstream and you have to get them

44:46 of your bloodstream and there's mechanisms that have to happen, but they are

44:50 primary infection fighters early on. They taken over later. Um 01 more

44:58 . So you might look at the , the cell types, they have

45:00 a weird um morphology. Well, , they look weird inside. They

45:07 these purple blobs. So this is , this is actually the DNA the

45:12 and, and they just form these like sacks inside, they're all

45:18 but that's just how they look. what they call them. Uh

45:23 uh nuclear polymorph like it means mini kind of nucleus. Uh It's kind

45:29 a weird fea feature of those Um basophils, basophils, unlike neutrophils

45:35 not fo cytic cell types. Their is to um release toxins typically and

45:42 types of uh cyto, right? so um yeah, so um lots

45:56 chemicals are released by basal pills, you see that the amount in their

45:59 is not, not that high. , uh if you have hay

46:03 things like that, you can probably your basal pills. Ok. Um

46:09 . So these are big acidic uh this big contributors as neutrophils, but

46:16 they do can act is in very pathogens. Not by large. I

46:21 , we talked about these worms right? Uh Those, those can

46:25 attacked by eosinophils. Their, their is often to produce lots of toxins

46:30 , and they actually interact with large . Um So again, large craft

46:37 to be something like a big helminth something like that, right? And

46:44 will be attracted to the site and actually interact with um have to interact

46:52 antibodies. So we'll see the antibodies interact with different of your immune system

46:58 in different ways. And so the are antibodies to the worm that eosinophils

47:07 also bind the antibody and then you these all together, it's a way

47:10 kind of uh collect a bunch of together. So that when they release

47:17 , right, you have a lot toxin. So it's a way to

47:22 theophil around a big pathogen, Because you're gonna have to like have

47:27 produce a lot of toxin and take of these things down. So if

47:30 can get a bunch of eins there have them hook on to the

47:33 then they release their toxin altogether and it down. So it's kind of

47:38 , how they work. Um but again, these little, these

47:46 things are investigated. A B is for antibody. OK. So like

47:51 said, you know, you'll, see interactions between draw antibodies kind of

47:58 this, right? Like a yay and, and these are all points

48:06 combine. So these, this part , the two that are close

48:10 those B antigen, the bottom part one that combined to a cell

48:15 right? Um, of some And if there is one type that

48:19 do that, there's others that you'll see as well. OK.

48:22 kind of jumping the gun here, because I'll, I'll repeat this

48:26 but just while we're here, it like a good spot. Um So

48:32 uh don't worry if we can get thing wrong because I'm gonna go through

48:37 again anyway, when we get the and antigens. Um So let's see

48:44 else is here. We got. OK. So a gran acidics,

48:48 are your uh macrophages, dendritic So, uh macrophages and dendritic cells

48:54 out as a monocyte. So monocyte circulate in the blood, but then

48:59 go to your lymphatic uh system. your lymphatic system plays a big

49:05 especially in your adaptive immune system. . So your B cells, your

49:11 cells, macrophages, dendritic cells, kind of hang out in your lymphatic

49:16 . That's what they do. So if you have, you had

49:19 infection and your doctor does this on throat, right? See the

49:26 right? Or maybe your armpits OK. And they get painful.

49:32 They're highly concentrated with lymphatic vessels, ? And so they swell because the

49:38 cell types in there are growing and right to fight the infection. And

49:42 what caused the swelling. Um the uh but they are so your your

49:49 and dendritic cells are py but also this function. Ok. They are

49:56 presenting stuff. So again, these cell types that link up with the

50:01 immune system and uh and uh they get activated by your active system uh

50:10 have other functions there, right? engine presentation is a big function um

50:17 really has to do with um to the body to intercellular pathogens. But

50:27 , I'll hold off on that. , we'll wait. But energy burning

50:30 or a PC, they're also called of short. Yes, test some

51:20 . OK. Now, very they are kind of trying to exploit

51:28 activity and expand it by genetically fixing killer cells to be able to be

51:37 at this function and recognize different types tumor cells. So using it to

51:42 a cancer fighting agent, OK. , there's a lot of work being

51:45 on that at the medical center on . Um But our context that we're

51:51 at uh cells are infected. So what happens is let me um

51:59 going to, I just need to real quick to see. OK.

52:02 it. Uh So the MH C , that's the thing we need to

52:07 about that affects a lot of different here. OK. So uh so

52:13 killer cells will look for infected or cells. So the thing is uh

52:19 , I'll elaborate here in a So your cells have uh certainly have

52:27 types of molecules on the surface. . I'm just, and one of

52:34 and they're supposed to, your, normal healthy cells have all different types

52:39 proteins on the surface, but they all have MH C Energen.

52:46 I'm just drawing them like this just , make it obvious. Um So

52:54 think of those as a barcode your, you, the there's a

52:59 on all of your cells that identifies as your cells, right? So

53:02 your own personal barcode on all of cells comprising all your tissues.

53:08 So, and they're supposed to be , OK? When they're not

53:13 that's the signal. Something's weird. not, right. OK. So

53:18 they're lacking or if there are only few this or this when they lack

53:26 have one or two, that's something . The body goes, that's not

53:31 . All right. And so that's natural killer cells look out for.

53:36 . And so they kind of, guess they kind of hover around the

53:39 and they can recognize if they've got usual stuff they're supposed to have,

53:44 ? These things and with lacking that's signal that cells do not what it's

53:49 to be something is wrong with Ok? I'll be infected.

53:54 And so infected cells like with a or other types, they can

54:01 not all of them, but many alter what happens on the surface of

54:05 cell, the type of cultures that up there. And that's what natural

54:09 cells, for example, can detect . And then the signal say get

54:13 of the cell, get it out the body, it's infected something's not

54:17 . But also cancerous cells can also that similar appearance, not all cancer

54:23 , but some can. And that is a signal of the cells,

54:26 normal to get rid of it. that's what natural killer cells do.

54:30 . Kind of look for that. I'll elaborate on MH C and in

54:34 second, but that's kind of what questions about that. So that's,

54:39 kind of what they do. So um and so when they do

54:43 , what do they do? they put this stuff in here uh

54:48 it easier, let's do this and . OK. So uh when you

54:58 to target cell, they will um these perforin. So perfer, so

55:07 of perforate, if you perforate you poke a punch a hole in

55:11 . OK? So perfer are kind like little straws, almost protein

55:15 they stick into the cell and the leaks up and they, and they

55:20 , OK? The enzymes are uh . These So apoptosis is a

55:28 Um It's a, it's a normal of all your cells. Uh It's

55:33 , it's what's called a programmed cell . So when your cells are,

55:37 age and they don't work right anymore something else damages them, the body

55:43 kill yourself, go through apoptosis. right? You had the sun

55:49 right? And you got, your was peeling. That's a way you

55:54 it was red, it probably hurt eventually the skin peeled. That is

55:59 a pop toast is going on. the uh ability come, what that

58:03 to is his so well have So you have two classes,

59:06 One and two. He's just wait I said uh uh 11 different,

60:13 how people interact uh with these uh different ways um and create different

60:21 OK? And those effects can the virus affect itself. OK?

60:27 it lacks m ac antigens. So will be gotten rid of.

60:31 Um The uh um other types interact um other t cell types interact with

60:41 , et cetera. We'll, we'll about that as we get into chapter

60:45 next week. OK. But the is MH C Engines, it's just

60:49 critical to have a system like right? Otherwise, if you had

60:53 infectious agent in you, how would body know that it's even foreign or

60:59 ? Right? So you already have system in place with all your pills

61:03 up all your tissues that have those stamped on them that are telling your

61:08 this is yours. Ok? So something else comes in that doesn't have

61:13 stuff, then your body can oh, that's something not right.

61:18 , foreign energy, right? Do with it. So that's having that

61:22 in place allows you to detect something not part of that system.

61:27 But of course there's even times when body will attack its own,

61:34 That's those, those are your uh diseases, right? So certain tissues

61:39 , you know, your body does them and that's, you know,

61:42 other different reasons. But nonetheless, a system in place like this allows

61:46 to detect something that's not, not same as what, what that is

61:52 pathogens of some sort. Ok. lymphatic system as mentioned is an important

61:58 . So it's not um in terms your uh immune uh immunity, the

62:06 uh you can check against different types , you know, things you breathe

62:10 things you eat. OK? Your your lymphatic tissue will um can be

62:17 dense in certain parts of your Like your spleen is particularly dense in

62:22 tissue, your armpits, your uh uh are very dense, your

62:27 area is very dense in this Um where your T cells, B

62:32 , macrophages, dendritic cells hang Ok. Um The uh uh the

62:43 and your spleen has dense lymphatic tissue filter out agents in your blood,

62:48 example. OK. Uh you have uh um lymphatic tissue with concentrated in

62:55 parts of your skin underneath your skin in your intestinal wall. OK.

63:01 so how a lymphatic system uh it's, it's a system of

63:05 of course, but unlike vascular there's not a heart pumping, in

63:13 , typically through gravity and through muscle and through the, the pulsing of

63:22 , your arteries and arteries and And so picking your arteries because lymphatic

63:27 are very close to these things. . And so that kind of assists

63:31 pumping fluid. Uh basically, with fluid, lymphatic system is designed for

63:38 to pick up fluid that's lodged from capillaries, right. So your veins

63:44 arteries um intersect very, very tiny cell, thick vessels called capillaries,

63:52 ? Called a capillary bed. And that's and these are concentrated in

63:57 in your vital organs. Ok. so it feeds them right? So

64:00 exchange materials in the capillaries, nutrients back and forth. And of

64:06 when that happens, you lose uh from your, you lose blood v

64:10 lose fluid from your your vascular So you have to be able to

64:14 that and dump it back in, ? That's what the lymphatic system

64:18 It collects that, what's called interstitial . Ok? It collects that and

64:24 it uh it dumps it back in around your clavicle, there's points where

64:28 dumps back into your cardiovascular system. so it kind of helps to maintain

64:34 and, and because you do lose from your cardiovascular system and that helps

64:40 it up. Ok. But also a place where your, these cell

64:46 reside. Ok. And so very for that. Um Now, here's

64:54 example of your intestinal uh kind of lymphatic tissue very dense in your intestinal

65:02 . Uh intestines is in these prish . OK. So very dense and

65:07 it looks like in there is you'll these kinds of what are called m

65:12 in between your normal kind of uh cells of the intestine that are about

65:18 food and things, right? And here are some microbes coming through,

65:22 have um immune system cells that neros things that engulf any kind of uh

65:29 microbes that are, that are in to get rid of them. And

65:32 you'll have these, there is a section and you see the dense tissue

65:37 here, pyres all throughout your OK. Um So here, so

65:46 tosis. OK. So again, is one of your main mechanisms fight

65:53 . OK. So your primary ones macrophages, dendritic cells and um

66:01 OK. And so in terms of , they uh can be what are

66:08 watering or fixed. OK. watering like the name applies, you

66:13 , you know, travel throughout your system. Uh uh watering around

66:18 you know, pathogens, what have fixed or stay in one spot.

66:23 , uh very common to have, example, alveolar macrophages that a lifetime

66:28 your lungs and they pick up any of uh microbes that might be

66:33 Um And so the uh granular sites neutrophils, right, infections early in

66:42 infection cycle, how this happens. first get macrophages are are figure to

66:57 cells to the site of affection. one, that's chemotaxis, then stick

67:03 the pathogens, right? That part that is the engulfment process. Take

67:07 in and then break it apart, it OK. So the four step

67:13 . And so um so here you , here's a macrophage. OK.

67:20 part of the binding process is these , right? So not just ingesting

67:28 sizing the cell but also releasing cyto blurt other cells in the body.

67:33 they have that as well. And so um optimization is something we'll

67:41 about later. And so the um sometimes you have microbial types that are

67:50 that bind easier and can be taken than others. Other types are are

67:56 have a very thick capsule. That makes them less able to be

68:00 and taken in, right? That's it's a Vance factor. And so

68:04 do you deal with that while you other chemicals that can code it and

68:08 that can be taken in. That's opsonin do, right. So something

68:11 antibodies complement these coat the pathogen and that's what's taken in, right?

68:19 it easier to fotis. Ok. um ingestion part. So you have

68:26 a vesicle. So it's engulfed right a vesicle called the PGA zone and

68:33 our feeding vesicle and then that fuses the lysosome. Ok? And that's

68:38 of a digestive organelle that will then down the microbes either through production of

68:45 radicals. We talked about that um these are toxic to the cell

68:51 also can have life design to break the cell wall and ultimately getting rid

68:55 it. OK. Now, the about a about this is these can

69:05 um the particles that are you see of these being released, these can

69:10 be be an MH C module and can present. And so microphage can

69:18 be an ancient presenting cell, A PC. And they can do

69:23 by taking some of this material combining MH C molecules in the cell than

69:30 to the surface. And now the is visible to the immune system that

69:37 can then respond in a different OK. That's what the antigen presenting

69:42 does for you. It allows the to see the engine and respond to

69:47 . OK, if I hadn't seen before. So um the uh so

69:54 just mentioned about OP IL optimization that everything is easily favor of th so

70:01 things like a big capsule typically So they enhance that you can produce

70:07 to it. And then those antibodies bound to the pathogen, right?

70:13 then the cell itself has a receptor can bind to that and the

70:20 right? And then the whole thing taken in, right. So it's

70:24 way to take something that that's not fit. Ok. Similarly, the

70:29 problems can occur, you can coat with uh antibody or complement complement are

70:37 of basically a soluble protein factors. , and so that can code the

70:44 and can change as well. So a way to take size things that

70:47 easily fixed with that. OK. , Opsonin are the molecule that

70:52 So it can be an antibody complement is the process technique this way.

70:59 ? Um That's a good way to the stop, right? Folks.

71:05 for hanging in there. Uh We'll you next weekend and uh go

-
+