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00:00 So I realized, uh because I was kind of a um last

00:06 not last minute, but, you , you may not have had

00:10 a lot of time to prepare for before, right? So I'm not

00:12 how many r even went through this or you just gonna give it a

00:15 over. That's fine. OK. we're gonna kind of begin with some

00:19 the basics uh in a way it of things that apply to the whole

00:25 . OK. So, uh of we're talking about. So the approach

00:30 we're taking is um uh how does body fight disease, right? And

00:38 , that immunity, then we look it from the other perspective of how

00:43 the pathogen? So by that time have learned all the different ways in

00:49 you can counteract infection, right? so then you look at,

00:54 well, how does, obviously it's , right? We get sick,

00:59 know. And so pathogens have ways get around all these different types of

01:04 , right? So that's what we at in chapter 25. And that's

01:08 , that's that um flip class So, um then we end,

01:14 end of it is kind of putting all together really, you know,

01:17 we look at different diseases and what mention. OK. Here, here

01:22 some of the ways you, you disease in the context of, of

01:26 particular disease and what, what the does to overcome it. So it

01:29 of puts it all together at the . OK. So uh innate

01:35 Um so we look at it in of one's own immunity, right?

01:41 you know, what is the state one's immune system? Of course,

01:45 to, you know, how susceptible are, you know, what's your

01:49 of resistance to disease? Ok. infection equal disease every single time?

01:56 it, we are well aware by of this particular group, all

02:03 what do we call those people? is a thematic characters, right?

02:10 . So, no, that's not equal. Uh Coke, Robert Coke

02:16 . But uh we learned that that's always the case. You, you

02:19 um good for meningitis organism. I almost half the population carries it in

02:27 throat and they have no symptoms of . Ok? But when an outbreak

02:32 , it's one of them. That's source of it. OK. So

02:36 so it's, that's true for many diseases that affect us. OK.

02:41 Mumps and measles um among others cold , et cetera. Uh any

02:48 Um So I kind of want to with this and why I mentioned it

02:54 several times this semester in various So that's a anybody know what that

03:01 from Chipotle? It's the burrito OK. So then we got avocado

03:08 on top of there, we got like lettuce looks pretty good.

03:15 I'm hungry. Um So, but know that um from 2016, I

03:22 it up 2016 2017 2018, 3 in a row was responsible for or

03:34 . Ok. Um And that, course, coined the phrase you can't

03:39 your coat without what is that equal ? Yeah, we call it

03:48 so it got so bad. So looked this up and it says um

03:53 from 2020 April. April 2020. uh three years ago, Chipotle agrees

03:59 pay 25 million in federal fines, ? So no, from 2015 through

04:07 . So 15, 16, 74 of food borne illness, outbreaks,

04:13 people sickened. Um I didn't say many people died. I'm sure there

04:18 a few deaths. Um the uh Chipotle uh 641 people in Boston.

04:28 . Ok. So um of course was it uh the the it was

04:35 to um people handling the food and hygiene, improper sanitation, right?

04:43 surprising. So, when you think uh and it related to um the

04:48 produce uh that they used and so learn this later, but you can

04:55 , you know, uh the farm the lettuce is grown and getting into

05:02 mouth on that burrito bowl, How many hands that change that went

05:07 ? Right? Distributor, that people picking it, distributors, blah,

05:10 , blah and anywhere along the you know, issue can happen.

05:15 , um, so what happens when have? Um, so there was

05:19 person who actually came was one of victims of this, right?

05:23 um and I have some stuff underlying . Oh, well, there's some

05:28 I wanna point out. So you know, Rita Bowl on October

05:31 became sickened. Four days later with diarrhea, uh common as we all

05:38 common G I tract infection symptoms, ? Uh registered nurse began experiencing buddy

05:45 , tell tale signs of an E infection. Stool sample tested positive for

05:50 toxin producing E coli. So uh here for a second and all right

05:56 and symptoms. So every as we , right, every focused on infectious

06:00 , right? Disease is due to acquiring a micro, right? Um

06:06 so signs of syndromes. So every has associated signs and symptoms,

06:12 Respiratory illness, you know, coughing in the throat, maybe these kind

06:17 things. G I tract infections all similar dehydrated when I lost some water

06:24 of thing. And so uh with cause of disease, every, every

06:30 disease has a cause ideological agent we it right. E coli, of

06:35 , it's a pathogen, um duration severity of the disease just went on

06:41 like uh typically for 10 days. stomach cramps, the fact that E

06:48 has, I remember this one This is the oh 157,

06:52 e coli uh virulence factors. Very . That's how pathogen causes disease,

06:58 for it. Uh The ciga toxin one uh I think is another one

07:04 attachment to your intestinal wall um and . And so it's what enable the

07:11 to do what it can do. many of these are evolved in overcoming

07:18 from your immune system. Ok? phase phase variation mechanism, right is

07:23 matter um reservoir, right? So source, right? So every infectious

07:33 has a reservoir reservoir is the source the, don't worry so much about

07:38 are kind of things we'll talk about 25. But um nevertheless, the

07:44 source. And so for e coli particular one, the source is actually

07:49 . Ok. Um We'll talk about later. How you know you go

07:55 , how do they get in my and how do they get it from

07:57 cow if everything less? Right? , there's that, that happens,

08:01 ? But um point is every infectious has a source and many times the

08:07 is a human, right? Like reservoir is a human mumps and

08:11 reservoirs are human. But for other , rabies, those are uh generally

08:18 , um bats, very common Uh anyway, the point is uh

08:23 are different types of reservoirs, They can be humans, they can

08:27 animals, they can be water or or just the depends uh transmission.

08:33 , reservoir is one thing, But it has to get to

08:38 right. Transmission of disease, various . Um food board, eating contaminated

08:44 , right? Water could be a uh when you transmit right um uh

08:53 right through the air. Very very that's probably the most common rou of

08:58 is through the air, right? I think of all the respiratory

09:02 right? Flu virus, the C , right? All those respiratory illnesses

09:09 uh airborne, right? And so uh so as we go through

09:16 again, this is kind of more 25 stuff, but that's the kind

09:19 at least get a preview of what do before we see what they we

09:23 do to them. OK. So , so the various factors the pathogen

09:30 , right? Various functions right? , I would say call this the

09:36 part of the infection here, Later part of the infection here,

09:42 ? So there is a kind of time element to it, right?

09:44 has to get in the host right? Maybe infect deeper into the

09:50 . These this is all things that time, but there's gonna be various

09:53 for each one of these things. . And so really how deadly a

10:00 pathogen is relates to a number of of factors. OK. So,

10:08 so again, this, we just in the context of that woman who

10:14 bowl, right? Uh pathology and is the process of causing disease,

10:20 ? So, infectious agents and their factors, et cetera, right?

10:24 we know that, you know, the infectious disease is, there's differences

10:29 terms of what they do to our , right, induces induce fever that

10:34 dehydrated, whatever, right? Rash all, it all depends all all

10:40 . OK. So um all So we'll get into the different,

10:45 let's see what we get to. , these are some easy questions.

10:48 think you'll, these are slam OK? Just kind of think about

10:54 , which responds faster, right? we look at adaptive and they just

10:59 of the organization of the immune Ok. Just a second.

11:21 OK. Let's count down 14, . Yeah, it's so think about

11:45 there's a pathogen right here is uh , COVID, right? What does

11:53 have to get through to cause Right. But how many layers,

11:59 . Well, COVID acquired through its transmission. So it's gonna go,

12:05 know, right? Mucous membranes, ? That's a, that's gonna be

12:08 physical barrier, right? Um Or it's something else maybe through the

12:14 skin is actually fairly impair, Yeah, you have natural openings and

12:18 . But um you know, airborne , right? So uh that's one

12:24 and then you go deeper, Then you have different cell types that

12:27 involved. Uh So let's just kind see the setup here. OK.

12:34 we refer to the each type. I think that's, that's three lines

12:39 defense, OK. Three lines of . First is your physical barriers,

12:46 mucous membranes, right? And your is nonspecific. OK? Whatever is

12:53 there, the physical barrier will stop , right? It's not specifically certain

12:57 OK? Um But that community the . OK. That community relies on

13:05 . OK. Recognizing antigen, that's it's all about. OK. And

13:11 a time limit to that, So we talked about that a little

13:15 in the context of the phase variation , right? It takes time to

13:20 uh seeing it's one thing then it buying to the engine, then it

13:26 a a um response, right? something will happen as a result.

13:31 all that takes time, right? is why in the immune system

13:36 of course, it's there much OK. So um first line

13:42 skin mucus membranes. But then remember both of these all right, skin

13:49 mucus membranes are bacteria, right? micro biotic enhance those two things,

13:59 ? So their presence, believe their presence also is a deterrent to

14:06 . OK. Um Third layer. if you get past that, now

14:11 get into more of what I call cell types and processes, processes kick

14:18 processes like the information like um um , I call these things processed,

14:27 involve chemical signals and step 12 and and these kind of things.

14:33 So, and then you have things compliment, these are non cell based

14:39 . OK? A compliment is um so um now once you get past

14:47 , then you have your third life that's your T cells and B

14:52 OK. So they're the ones that involved in recognition, but you do

14:58 um uh cell types that will work both sides. OK? And that's

15:09 that's your uh dendritic cells and So they have, they have um

15:18 in both on both sides. These can actually work with um key

15:26 . OK? And so the B are the ones that produce antibodies.

15:32 . T cells have a little bit function in actuality, certain T cells

15:38 of control the whole process. Uh But that's what we'll talk about

15:42 . Um we'll talk a little bit it today and next time, but

15:46 chapter 25. OK. So um three levels right now, uh

15:55 her, that immunity is all OK. Remember that can be what's

16:03 the periphery, right? Uh is it a gram gram out of

16:09 , the molecule sticking out of A virus and like the protein

16:14 envelope proteins. Um uh a flagellum ? Things that are on the

16:20 So uh let's look at this Should be another easy one. All

16:29 . So, among your family who do you think forgiving you,

16:37 microbiota such a thunderous sound? All . This can down from 10.

17:17 let's see. Let's see. of course. It's your mother.

17:22 . Mother's day is coming up, your card. Thanks for the

17:26 OK. Um Among other things, . So um when you were

17:34 obviously, it require me that microbiota birth. OK? Um Thereafter,

17:43 acquiring other types, right? Because you're in the environment, right?

17:50 in the air, things you eat these are all gonna be contributing to

17:55 microbiota as you grow up. And so uh here this table is

18:01 showing you and don't memorize this but it's just showing you kind of

18:05 numbers of these, right? So skin uh 10, 10,000 um 1000

18:18 per mil, right? C F is what we call form a

18:22 So basically think of C F U cell. So mil so the amounts

18:28 per line, for example, uh the mouth, the uh millions of

18:37 , the uh G U track, the G I track, right?

18:41 to the 11th per cubic centimeter. a humongous amount of bacteria in your

18:48 . OK. So uh now I saying, OK. Yeah, they're

18:54 everywhere, right? They're found everywhere your body well, they shouldn't be

18:58 , right? They shouldn't be floating in your brain, for example,

19:01 your heart, right. That signals signals some type of infection.

19:05 you know, aside from your vital , they are pretty much everywhere.

19:10 ? And they have their specialized micro environments. Ok. Uh They'll

19:17 . You'll have some certain types on skin you're not gonna have in your

19:22 . Ok. Many, you many will be aerobic, some

19:26 OK? Um But they create their little micro environment. So even in

19:31 mouth, your mouth, you'll have ropes in. There you go.

19:35 you're breathing air around them all the , right? Well, because they

19:39 , they're tiny, right? They hide mix and crannies in your,

19:42 your teeth, right? Your gums what not. That's how you get

19:45 cavities from bacteria. OK. So they ferment, right? And remember

19:51 need, you need to be anaerobic throw in for me. And so

19:54 , there's places that hide your mouth are anaerobic, you can't really create

19:57 OK. Uh environment. And so the skin typically is kind of salty

20:03 that attracts environment for staff, staff , can, can withstand higher salt

20:10 . So the point is all parts your body have these different micro environments

20:14 different types of, you know, terms of P H and so concentrations

20:19 salt concentrations, et cetera and the that inhabit those areas are very well

20:24 to them. Ok. As they be, as you want them to

20:28 , right? Because this principle of you learn, I, I assume

20:32 , by a one on the ecology there. Um, a criminal

20:38 Ok. Well, no, you heard it as competitive exclusion, but

20:42 mean, same thing, right? I think what's the textbook definition

20:47 No, two species can occupy the niche, right? Once you gotta

20:52 or be eliminated, right? And out. OK. And that's,

20:57 that principle is what helps keep, , helps keep pathogens out of your

21:02 or you have a well established microbiota something just to plop down and take

21:10 that can be very hard. When that can happen, what makes

21:15 easier for types to assert themselves and is this you're an antibiotic that can

21:23 the levels of, of your micro and that could open up opportunities for

21:29 . So that's one example, But you know, you're a healthy

21:34 , you're not on an inbox or , then you want that microbiota there

21:39 thing. OK? And so you look at these symbiosis, I'm sure

21:44 familiar with this. You, you um assign a zero plus or

21:50 to each member of the symbiosis, ? And so it is, and

21:54 of your microbiota falls into the first categories. OK? And mostly

22:02 but certainly those that are mutual. . So um and every day there's

22:09 new about one's microbio, right? everything from uh supplying you very effective

22:17 and amino acids to uh allowing you digest certain foods you otherwise couldn't because

22:24 can to immunological effects, positive immunological , um everything it could be like

22:35 effects as well. Like because remember those millions of micro micro microbes you

22:40 in the body that's millions of other you've got as well, so to

22:47 , right? And so the effects those, we understand some of

22:51 but there's a lot we don't And so um but think about how

22:56 they've been with us, right? have been evolving for six million

23:00 You've had that you had those bacteria humans, of course, the same

23:04 of time. So of course, gonna be some for the most

23:08 right? Um helping each other out . Um That's why I say you

23:14 , you can't be a germaphobe, ? You want those, you want

23:18 OK? Um The parasitic types, course, uh you can prior to

23:25 . Um obviously the parasites uh benefiting at your detriment. So, but

23:32 , uh commences mutual types. Those what pretty much make up your

23:38 but even those types, right? these guys, all right, every

23:43 in a while can become one of OK? Opportunistic. OK. Staff

23:51 a common example of this, You have staff primarily in your,

23:56 just memorize your nose skin. but if new areas open up to

24:04 , right, they can get beyond normal environment where they're more or less

24:08 a check and that's kind of where like to go. But if they

24:12 new entry to a cut or then you can have issues.

24:18 So now they're in areas they don't belong without the normal checks on them

24:22 they can proliferate uh not all but there's certain types that can do

24:27 . And so uh that's when a was once thought to be a mental

24:34 mutual type becomes an opportunistic pattern. . So uh that's so the primary

24:41 , right? Very different, The primary pathogen, if it's there

24:47 your body, it's not there just hang out, it's there to cause

24:51 , right? So primary pass something Ebola um anthrax um number of

25:00 right? So these are part of normal microbiota, obviously. OK.

25:06 , um all right. Any questions this? OK. All right.

25:13 let's look at, so it's gonna a little bit redundant because we look

25:17 physical barriers, we can look at in the context of being a physical

25:23 . But then also they have this function, which is being a chemical

25:27 because these physical barriers also produce secretions these secretions have chemicals that can have

25:37 activity. OK. So they kind have dual functions here. So,

25:41 the context of physical barrier, Skin obviously uh skin again is a

25:48 protective layer. OK. Um Thick remember it gives your cells stack on

25:54 of one another, right? It carrot, that kind of helps really

25:59 it, right? And so it's easy to penetrate through skin,

26:06 But the only way that happens is an insect vector, right? An

26:10 , uh what's not a virus, example, right. So the the

26:14 itself penetrating your skin through its uh . Um but you know, you

26:22 have natural openings obviously in your right? Pores, right? Sweat

26:26 , et cetera. That's where bacteria get in. Um when we talk

26:30 subcutaneous infection, that's usually introduced like a wound to some type of splinter

26:37 . What have you, then you get a subcutaneous infection um which can

26:42 be through a uh an opportunistic pathogen then arise this way. Ok.

26:50 , uh so mucous membrane. So are gonna be the line,

26:54 Your your body cas right? Not your nose and your throat and your

27:00 , right? These are all uh membranes. And so um that's a

27:05 as well. OK. And so uh have, for example, uh

27:12 and your mucous membranes have to be moist, right? Hence mucus,

27:17 ? That's what that mucus secretion is . And so uh uh tears and

27:22 , right? So saliva washing over teeth creates the contain, clean,

27:27 off your teeth of, of, microbes, um tears, you

27:32 you produce tears for the same function hairs in your nose and ears,

27:39 ? Um Help you keep stuff right? Trap dust, trap particles

27:44 whatnot. Um But especially this one escalator. Ok. So this is

27:52 your uh trachea or windpipe if you . Ok. Full of little hairs

27:59 are really moving, but it's that the mucous secretions that serve the

28:06 particulates get them out um when that's , right? Which, which

28:11 which it can be in, in illnesses. Ok. That stuff can

28:17 get into your lungs, right? often. Uh you might have

28:22 a uh primary infection due to a , right? Say a cold,

28:27 cold or flu in the course of infection, you become uh dehydrated,

28:36 ? Very common. What do what do you, what do you

28:38 told when, if you have a or a cold, drink fluids,

28:41 fluids, right? Because you get and if you, we normally don't

28:45 enough when it happens, it affects mucus um consistency. So it doesn't

28:52 as well. So it's not uncommon have a respiratory environmental infection that then

28:58 followed by a bacterial secondary infection. much worse because now it gets into

29:02 lungs. And um like pneumonia is , an example of that,

29:08 So the point is this is a important defense to keep functioning right?

29:15 in order to counteract a respiratory Ok. Um So other things you

29:22 go OK. What, how does have any use? Right. How

29:24 the ear wax? How does that me out? Well, it's it

29:28 , trapping stuff in there, Um Digestion, you constantly, your

29:33 are constantly about paralysis, right? material for your gut. Ok.

29:39 of course, covers the windpipe when swallow. So you don't get food

29:43 your uh trachea. So any these are all again, physical

29:48 but they all produce uh certain right? Chemical defenses, right?

29:55 , just the nature of the skin , very oily. Um although it

30:00 from person to person uh kind of . So these are environmental conditions that's

30:05 suitable for, for many microbial ok? Uh mucous membranes,

30:12 Saliva, gastric juice, low P and started by two um urine uh

30:19 slightly acidic. Um but a common is this, you see the multiple

30:27 Lyo design, right? So the apart pep, right? So it's

30:32 defense against bacteria. OK. Um defense and so defenses are produced by

30:42 lot of different cells in your right? They're just little short uh

30:48 um that basically acts like a it kind of goes into the membrane

30:55 leaks, right? And so there's of different types of defenses, hundreds

31:00 them, I think that various of cells produce uh your macrophages, your

31:07 um cells which are your, one your primary big acidic types have them

31:11 well as other types of cells in body. So um so just from

31:16 alone, physical barriers, chemical you get a lot of stuff already

31:22 can, that can counteract uh OK. Um Now one of those

31:31 fits in this category too, what call toll like receptors. So the

31:35 I think of these things is as alarm bells, let's the fire alarm

31:40 your body, right? Signaling something be going on here, infection

31:46 OK. And so of course, the way your body tells alert cells

31:53 your body through chemicals, right? signals is how your body talks to

31:58 cells, right? And so this uh it used to be called

32:05 OK. Now it sounds weird, it became maps. OK.

32:12 The maps. Uh oh to me it is is to me it kind

32:19 signals an action basically. OK. they call them maps. OK.

32:23 these are uh typically amino acid uh or sequences in these different types of

32:31 of flagella, the cell wall, LP S layer, et cetera.

32:36 amino acid sequences are recognized in these structures and they bind to a receptor

32:42 that binding generates a chemical signal. . So you have types that external

32:51 internal receptors, right? So your like receptors T L R S are

32:58 the surface, right? The other are what we call nod like

33:04 they're internal. So remember uh bobby , virus like a virus can infect

33:11 be inside of a cell. So some of those things can be found

33:17 by a nod like receptor and create effect. Ok. Um So here's

33:23 example of pathogen, right? There's bacterial pathogen and the flagellum part of

33:31 can act as a as a right? And internally. So say

33:38 have a, so the way toxins is bacter toxins, they get inside

33:43 cell and cause different effects. So in itself can also be an N

33:47 . So can a viral infection, of those can, can uh bind

33:52 these. And so whichever one it's to, it's gonna create this cascade

33:58 them, right? Basically, the the production of different signals that ultimately

34:04 lead to production of cytokines. And is something we'll, you'll hear time

34:09 time again in this unit is cyto , cytokine site. So it's a

34:15 term that describes a number of different which have various roles in fighting an

34:23 . Ok. And those roles there are some, not all of

34:27 , but some of the major So chemo attractive. So you have

34:32 infection somewhere. You want to bring the relevant cells that can take care

34:37 the infection to the site. So have to attract them and track them

34:41 the certain chemicals. Another important function um basaltic factors. Ok? Especially

34:52 . Ok. Your major cell pathogen fighters are neutrophils that are in

34:58 blood neutrophils, right? They go then ingest, right? So your

35:06 has like is full of like 70% your blood is is neutrophils.

35:12 So they're of course, circulating in blood vessels. So what you need

35:18 an infection, you need to get out of the blood vessels.

35:24 To do the job. And so where vasoactive factors can they manipulate blood

35:30 , making them more leaky, enable to come out, right? And

35:36 so very important function. So we'll that in the inflammatory response, we'll

35:41 about next time. Uh activating T activating macros, these are important infection

35:48 . So, t cells will activate adaptive immune system. Let me get

35:53 going. So, so, and are just 44 different types. There's

35:58 more than that, each with slightly different roles, inducing fever for

36:04 kind that do that. So very functions, all, all with the

36:08 of, you know, in some or another counteracting an infection.

36:15 Uh Basically telling other cells of the system to do different things to,

36:21 overcome this infection. OK. And , um so again, it's the

36:25 you hear a lot, you'll hear lot in intersection of and so,

36:30 so let's look at this question. . This won't be too difficult.

36:37 , you got the, uh, pictures. Wait, is there another

36:42 here? Hold on. All Yeah, of course, we have

36:47 , I think of it. All . So we got, uh,

36:51 have trophy, the macrophage and at site don't have a picture of a

37:00 . Yeah. If you're looking for cell of the adaptive immune system,

37:04 a name, a general name for . Ok. Let's count down

37:59 Um OK. See. Yeah, gonna be the sites of course.

38:10 . So uh T cells, B that fit into the lymphocyte mode.

38:16 . Um So we look at, we go from physical chemical barriers to

38:23 second line even. So different cell , specific cell types. OK?

38:29 So you take blood, of I'm sure you know this you can

38:33 , right? You'll have a uh fraction and a uh uh fraction um

38:41 set uh pellets. OK. And we got at the plasma which is

38:46 protein, heavy blood plasma contains basically of protein. OK? Including

38:52 complement and other um formed elements are cells. So erythrocytes, red blood

38:59 , leucocytes, that's our focus Um And so the term granular site

39:06 a granular site, all that refers is how it looks under a

39:11 OK. Granular sites have very obvious in them. OK? A grano

39:19 do not but it doesn't mean they have them. They're just not as

39:23 and visible in the light microscope. really the only, that's the difference

39:27 those two terms. OK. Um they look like under a microscope.

39:32 . So neutrophils basophils Eoin, Um lymphocytes are in the a on

39:41 side side. OK. So let's at some of these more closely

39:47 So neutrophils primary big city type early the infection. OK. So early

39:55 is a very, they have a kind of uh nucleus uh that we

40:02 load different loads. It's all connected they appear as like lumps or

40:10 single movie that they very characteristic in group. Um These are types that

40:17 blood that is again early early in infection cycle. They're the primary ones

40:22 the work. Ok. Um So are not about, they're much less

40:30 in the cell in the blood, me. Um They, they often

40:36 um antibodies sitting on top of Ok? And those antibodies will bind

40:44 and that will create an effect in basophil. Basic basophils are about emitting

40:50 . That's what they do. Um like histamine and others are part of

40:54 inflammatory response will talk about that But they thing about really chemicals.

40:59 you have allergies, these kind of overactive and that's when you get your

41:04 watery eyes and, and, and these can be acidic but their function

41:18 really with dealing large pathogens by I mean large could be multicellular

41:24 right? You can have infectious agents are things like worms, right?

41:30 so these tend to deal with those , ok? But again, they're

41:35 heavily a toxin releaser, ok? Among the leucocyte, a, I

41:43 say a grand you've got um monocytes typically are floating in the blood,

41:52 then they exit and go into your tissue. Lymphatic tissue is kind of

41:59 of it as a a it's in to your circulatory system, OK?

42:05 a system of vessels, OK? you have lymphatic fluid going through

42:10 We'll talk about that next time, that's where they develop into macrophages and

42:16 cells. OK? In this lymphatic , um these have a role as

42:22 mentioned in working with the adaptive immune . OK? A a function they

42:30 is what's called antigen presentation. And it's that function that kind of

42:39 them to the adaptive immune system, they work with cell to that

42:43 OK. Again, we'll elaborate on later. But um the, the

42:50 uh natural pillar cells are also a of lymphocyte um as well as T

42:58 and B cells. OK. uh so you differentiate T cells and

43:05 cell function in terms of what they , you gotta remember, um pathogens

43:14 be of two types, they can their disease cause stuff completely outside cells

43:22 exercise that right. Um Then there types that do not they go inside

43:30 , the obvious example there of But you haven't learned this yet,

43:36 you'll learn that there are also bacterial that can also go inside cells,

43:43 for the purpose of replicating cells like virus does, but to hide

43:48 hide out from the immune system and to penetrate deeper into your body.

43:56 the meningitis organism typically sits on the , right on the um mucous

44:02 OK. But then it gets into brain, right? So how does

44:07 do that? Well, it has to get inside your different cells and

44:13 to the brain. OK. So a type of intracellular pattern.

44:19 Um So the point is that viruses definitely are of that inciter type

44:26 so too can certain types of bacterial . OK? As we'll learn.

44:29 right. So you have to have that will deal with both types.

44:36 ? And um that works can work differently. OK. So you have

44:42 cells that, that's kind of their to do that. And then B

44:46 produce antibodies. So, antibodies, , which we always draws like these

44:51 shaped structures, right? They recognize on this part of the antibody.

45:00 . A G is short for OK. So then you have a

45:04 here, they actually combined to a , right? But um the engine

45:10 , this these only work outside the and anybody can't go inside of the

45:17 . And interact with an manager. only work outside the cell. The

45:21 cells are ways of dealing with uh that have been infected. OK.

45:26 we'll see. All right. um the natural killer cells,

45:33 So these are the type, they a type, they can recognize infected

45:38 . OK. Remember it could be virus infected cell. How you

45:43 how you gonna know that? Because not inside the cell being recognized,

45:47 inside the cell hiding. So you to have a way to, to

45:50 those type types of cells that are . Ok. Um Also some cancerous

45:58 uh can be recognized by natural killer in. OK. It's actually an

46:04 , has been an active area of is to take advantage of this,

46:10 ? In terms of using it to with different types of cancers.

46:15 Um OK. I don't, I not. We're gonna talk about these

46:22 . All right. Any questions? how I'm gonna, that's what we're

46:26 stop here today, folks. Pick up next time. Thanks. Have

46:31 good weekend. Go

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