Referat Sistem Imunitas Kulit
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Transcript of Referat Sistem Imunitas Kulit
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Sistem Imunitas Kulit
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Struktur kulit normal Sistem imunitas kulit
-innate immunity-IL-1-aktivasi komplemen-PRRs -sel Langerhans & dermal DC-acquired immunity-peran sel T & B
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Kulit Normal
Terdiri dari tiga lapisan-epidermis memiliki ketebalan 150 µm
Stratum corneumStratum lucidumStratum granulosumStratum spinosumStratum basaleMembran basal
-Dermis ketebalan 2,800 µm -Subkutis (hipodermis)
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Struktur Anatomi Kulit
1 Epidermis
2 Dermis
3 Subkutis
4 Folikel rambut
5 Glandula sebasea
6 Sweat gland
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NORMAL SKIN STRUCTURE1. Stratum corneum2. Stratum lucidum3. Stratum granulosum4. Stratum spinosum5. Stratum basale6. Membran basal
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NORMAL SKIN STRUCTURE
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
keratinocyte express epidermal growth factors : amphiregulin
-induce inflammatory-immune reaction-recent finding expression amphiregulin by Th2 important mechanism to clear intestinal helminth infestation through epithelial shedding
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INNATE IMMUNITY
epidermal γδ-T cells, like B cell, capable directly binding to small phospate containing Ag with their receptors-do not require Ag presentation in context of MHC or CD1-serve as primitive, immediate response element, recognizing conserved phosphoprotein or phospholipid Ag of microbes & necrotic human tissues
B.Spellberg.Life Sciences 2000;67:477-502
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NORMAL SKIN STRUCTURE
B.Spellberg.Life Sciences 2000;67:477-502
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CUTANEOUS IMMUNOLOGY
Innate immunity-first-line defense mechanism-two separate categories
-constitutive innate immunity-anatomic barrier
-physiologic barrier
N Franklin. Middleton’s allergy 7th edition 2009
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CUTANEOUS IMMUNOLOGY
-inducible innate immunity-acute inflammation-cellular infiltration
-both do not demonstrates acquired specificity or memory for invading pathogen
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
1.cutaneous constitutive innate immunity consist of
1.1.normal skin flora1.2.cornified keratinocytes1.3.antimicrobial polypeptides/lipids1.4.low pH1.5.normal body temperature
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
Normal flora of skin-coryneforms and staphylococci -mush lesser extent, fungi (primarily Malassezia)
Compete with other pathogenic organisms
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
Cornified keratinocytes -form impenetrable surface-outward growth and shedding of cornified keratinocytes eliminate superficially bound pathogens-reduced water content & lipid layers of stratum corneum reduce relative humiditybad environment
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
Antimicrobial polypeptides -β-defensin-1 and -2, dermcidin, iron-binding proteins, lysozyme, RNases, DNases, and natural IgM on skin from sweat and from keratinocytes
Reduce skin surface pH-exhibit antibacterial activity-lactic acid excreted in eccrine sweat
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
Normal body temperature -inhibits growth of some pathogens
2.Inducible innate immunityAcute inflammation2.1.performed IL-1α stored in cytoplasm of keratinocyte,released from
itch/scratch2.2.TNF-α
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
IL-1-2 forms : α and β-31 kDa molecules-IL-1β must be cleaved by ICE
(IL-1β converting enzyme : caspase-1)-produced by monocyte, MØ, langerhans cells, dendritic cells
-IL-1α biologically active predominates in epithelial cells (keratinocytes, etc)
Murphy JE. J Invest Dermatol 2000; 114:602-608
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INNATE IMMUNITY
-receptors-IL-1R1 can bind both IL-1α & IL-1β-IL-1ra(IL-1 receptor antagonist) bind to this Rc but does not induce signaling
-mice defcient in IL-1ra show exaggerated & persistent inflammatory responses
Murphy JE. J Invest Dermatol 2000; 114:602-608
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INNATE IMMUNITY
-IL-1R2 -short cytoplasmic domain -bind IL-1α & IL-1β efficiently-but not IL-1ra-serves to inhibit IL-1 responses-expression can be upregulated by corticosteroids & IL-4
Murphy JE. J Invest Dermatol 2000; 114:602-608
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INNATE IMMUNITY
Murphy JE. J Invest Dermatol 2000; 114:602-608
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
-important among this cascade of events is induced expression inflammatory cytokine, chemokine, mediators(eicosanoids, histamine, neuropeptides, ROS)-contribute to classic signs of acute inflammation : redness, heat, swelling, pain
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
IL-1α induce molecules of typical cutaneous inflammatory response include : TNF-α, IL-8(CXCL-8),
nitrous oxide synthase, PG-producing cyclooxygenase, postcapillary venule endothelial cell expression of ICAM-1, VCAM-1, E-seletin
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
-Moreover,IL-1α & other induced molecules activate most cell types of skin, alerting and preparing them for further host defense functions including cytokine and chemokine secretion, wound repair, release of antimicrobial products, phagocytosis, initiation of acquired immune responses
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
2.3.inducible pathogen-targeted soluble molecules
-inducible antimicrobial polypeptides-complement-activating a/o opsonin proteins-complement proteins
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
Inducible antimicrobial polypeptides-β-defensin-2 and -3, cathelicidin LL-37-produced by keratinocytes-IFN-α, IFN-β, IFN-k another class of antimicrobial polypeptides(IFN-α produced by plasmacytoid DC, mononuclear phagocytes)
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
-IFN-β produced by many cell ; fibroblasts sometimes called fibroblasts IFN)-protective activities related to antiviral effect on host cells rather than diract toxic to pathogen
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
2.4.complement activating/opsonin molecules-members of acute phase proteins (C-reactive protein, serum amyloid protein)-members of collectin(mannan-binding lectin)-ficolin lectin families-C3b fragment, natural IgM
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
2.4.complement activating/opsonin molecules-acute phase protein produced by liver & supply to skin via blood-increase serum concentration in response to IL-1, IL-6, TNF-α from activated MØ-collectins & ficolins recognize carbohydrates on bacteria, fungi, viruses then mark them for destruction
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
-opsonin C3b target pathogen : phagocytosis-C3a, C5a(anaphylatoxins) : keratinocyte activating, chemoattractant, mast cell degranulating functions)-C5b, C6, C7, C8, C9 : MAC(lethal pore)
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INNATE IMMUNITY
N Franklin. Middleton’s allergy 7th edition 2009
2.5.PRRs host molecules recognize -PRRs host molecules recognize PAMPs -PAMPs include
-unmethylated CpGs of bact. DNA-dsRNA(e.g.influenza)-mannans-gram+ bact. lipoteichoic acids-gram- bact. LPS-bacterial peptidoglycan
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INNATE IMMUNITY
2.5.PRRs host molecules recognize(cont.)-N-terminal formyl-methionine-parasitic phosphoglycans-fungal glucans/zymosan
-MØ & DC ,activated during cutaneous inflammatory response, first phagocytic host cells utilizing their cell-surface PRRs
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
-inflammation-ass increase chemotactic factors (chemokines), produced by keratinocytes stimulated via their TLRs and postcapillary venule endothelial cell adhesion molecules (P- & E-selectin, ICAM-1, VCAM-1) synergiscally mediate integrin-dependent extravasation of PRR-expressing leukocytes
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
-cellular infiltration -neutrophils earliest infiltrating leukocytes(due to neutrophil active CXC : IL-8)-later, monocyte begin extravasate into inflam. site-assist in phagocytosis & intracellular destruction of pathogen with lysozyme, defesins, ROI
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
-eosinophil less phagocytic than neutrophil, produce ROS at plasma membrane surface, not intracellularly readily degranulate & deposit toxic cationic proteins onto surface of parasites-furthermore : basophils, blood Dc, mast cell, T cells, B cell, NK-T cell, NK cells
N Franklin. Middleton’s allergy 7th edition 2009
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INNATE IMMUNITY
-local defenses are quickly augmented by recruitment of dermal MØ, just beneath basement membrane-lymphocyte-/keratinocyte-derived IFN & growth factors across basement membrane initiates priming MØ to produce IL-12
B.Spellberg.Life Sciences 2000;67:477-502
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INNATE IMMUNITY
-epidermal-derived cytokine & Ag stimuli MØ mobilize their cytoskeletons to become mobile & secrete metalloproteinases and degradative enzymes allow them to slice through collagen and other structural components of basement membranecross into epidermis
B.Spellberg.Life Sciences 2000;67:477-502
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INNATE IMMUNITY
-MØ use ligands expressed on activated keratinocytes, such as E-cadherin/ICAM-1, to pull themselves through epidermis and crawl to danger site by following chemokine gradient to its source
B.Spellberg.Life Sciences 2000;67:477-502
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INNATE IMMUNITY
B.Spellberg.Life Sciences 2000;67:477-502
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INNATE IMMUNITY
B.Spellberg.Life Sciences 2000;67:477-502
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ACQUIRED IMMUNITY
-inflammation state that continues beyond 24-36 hr induces onset of adaptive immunity-IFN-γ in epidermis stimulates leukocytes, fibroblasts to express CC chemokines, particular MCP-1, MIP-1, RANTES while suppress production of CXC chemokines such as IL-8
B.Spellberg.Life Sciences 2000;67:477-502
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ACQUIRED IMMUNITY
-MIP-1α : CCL20;induce chemotaxis of neutrophil and lymphocytes-MCP-1 : chemotactic for monocytes & lymphocytes-RANRES : selectively pro-inflammatory Th1 lymphocytes, not inflammatory-suppressive Th2 cells
B.Spellberg.Life Sciences 2000;67:477-502
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ACQUIRED IMMUNITY
-Th1 have RANTES Rc : CCR5-Th1 produce IFN-γ which drive RANTES production by lymphocytes and MØ selectively summon additional Th1 cells to area of danger
B.Spellberg.Life Sciences 2000;67:477-502
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ACQUIRED IMMUNITY
-endothelial cell adhesins critical to selection of leukocyte extravasation-several hour after stimulationlower their expression of E-selectin(CD62E), upregulate their ICAM-1 expression, begin express VCAMdiminish neutrophil across vascular lumenL & Mo are recruited into area
B.Spellberg.Life Sciences 2000;67:477-502
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ACQUIRED IMMUNITY
-exposure to IFN-γendothelium express MHC class II
then presence of IFN-γ, microvascular endothelial cells capable acting as professional APC to circulating T cells
B.Spellberg.Life Sciences 2000;67:477-502
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ACQUIRED IMMUNITY
-In presence in skin of IFN-γ, IFN-α, TNF-α, microbial particles (LPS, gram+ cell wall fractions, prokaryotic DNA)induces MØ & DC produce IL-12-IL-12 induces newly activated T cell to Th1
B.Spellberg.Life Sciences 2000;67:477-502
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ACQUIRED IMMUNITY
-if stimulus initiating danger response is too bulky(hyphal fungi, helminths, large foreign bodies,etc)leukocytes initiate “frutrated phagocyte complex” this induce production of IL-10 prefentially over IL-12favoring antibody-based Th2
B.Spellberg.Life Sciences 2000;67:477-502
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ACQUIRED IMMUNITY
-antibody production stimulated by Th2 response allow leukocytes to damage large organisms via ADCC-eosinophil, neutrophil, NK, monocyte/MØ able to use this mechanism
B.Spellberg.Life Sciences 2000;67:477-502
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ACQUIRED IMMUNITY
-B cell other key cell for acquired immunity-B cell recognize relatively intact Ag (contrast T cells)-plasma cell, memory B cell development, Ig class switching, somatic hypermutation all occur in secondary lymphoid geminal center of skin-draining LN
N Franklin. Middleton’s allergy 7th edition 2009
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ACQUIRED IMMUNITY
-absence of cutaneous B cells suggests a need for Ag that enter skin to be transported to B cell as opposed to B cell’s migrating to Ag in skin(but mechanism of B cell activation remains unclear)-five classes of Ig have been detected in normal human sweat
N Franklin. Middleton’s allergy 7th edition 2009
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ACQUIRED IMMUNITY
-sIgA arise from secretory epithelia of eccrine glands, sebum also contain IgA-exact source of cutaneously secreted Ig remains unresolved-IgG1 & IgA capable to clear pathogenic organisms from skin via Fcγ Rc-mediated immune response(ADCC, complement fixation) and sIgA-coating of bacteria
N Franklin. Middleton’s allergy 7th edition 2009
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ACQUIRED IMMUNITY
-in human IgE & IgG4 produced by type 2 cytokine (IL-4, IL-13)-most antigen-specific IgE supplied via blood(except respiratory mucosa , local IgE production appear posible)-IgE can bind to FcεRI-bearing cells(LC, mast cell, infiltrating basophils)contribute to various allergic skin dz
N Franklin. Middleton’s allergy 7th edition 2009
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ACQUIRED IMMUNITY
-Ab specific for FcεRI may contribute to cutaneous dz such as urticaria, Ab against desmosomal and hemidesmosomal protein provoke immunobullous dz
N Franklin. Middleton’s allergy 7th edition 2009
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ACQUIRED IMMUNITY
-impact of innate to acquired immunity-chemotactic activity of β-defesin-2 & C5a for DC a/o T cells-tissue injury danger signals or engagement of PRRs(LPS Rc, mannose binding Rc, TLRs, CD1a) expressed on cutaneous APC such as Langerhans’ cells, dermal DC, MØ
N Franklin. Middleton’s allergy 7th edition 2009
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ACQUIRED IMMUNITY
increase co-stimulatory molecule expression (CD80 & CD86) & modulate
cytokine expression patterns-LPS bind to cell surface CD14 of MØ induces IL-12favor Th1 development-mast cell-produced cytokines such as IL-4, histamine, keratinocyte-derived thymic stromal lymphopoietin(TSLP)acquire immune response Th2 profile
N Franklin. Middleton’s allergy 7th edition 2009
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ACQUIRED IMMUNITY
B.Spellberg.Life Sciences 2000;67:477-502
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SUMMARY
N Franklin. Middleton’s allergy 7th edition 2009
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TAKE HOME MESSAGE
-Various constitutive and inducible innate immune mechanisms function in skin to fight infection and to direct acquired immunity – these include keratinocyte– derived molecules such as IL-1, antimicrobial peptides -Immune functions attributed to cutaneous mast cells and dendritic cells (DCs)
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TAKE HOME MESSAGE
-Langerhans' cells, dermal DCs, and DCs infiltrating during inflammatory disease are increasing in number and being redefined-Skin homing of memory, effector, and regulatory T-cell subtypes is programmed by skin-derived DCs and prominently directed by CLA,other types of chemokines