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Type iv hypersensitivities

Type IV hypersensitivities are not mediated by antibodies like the other three types of hypersensitivities. Rather, type IV hypersensitivities are regulated by T cells and involve the action of effector cells. These types of hypersensitivities can be organized into three subcategories based on T-cell subtype, type of antigen, and the resulting effector mechanism ( [link] ).

In the first type IV subcategory, CD4 T H 1-mediated reactions are described as delayed-type hypersensitivities (DTH) . The sensitization step involves the introduction of antigen into the skin and phagocytosis by local antigen presenting cells (APCs) . The APCs activate helper T cells, stimulating clonal proliferation and differentiation into memory T H 1 cells. Upon subsequent exposure to the antigen, these sensitized memory T H 1 cells release cytokines that activate macrophages, and activated macrophages are responsible for much of the tissue damage. Examples of this T H 1-mediated hypersensitivity are observed in tuberculin the Mantoux skin test and contact dermatitis , such as occurs in latex allergy reactions.

In the second type IV subcategory, CD4 T H 2-mediated reactions result in chronic asthma or chronic allergic rhinitis . In these cases, the soluble antigen is first inhaled, resulting in eosinophil recruitment and activation with the release of cytokines and inflammatory mediators.

In the third type IV subcategory, CD8 cytotoxic T lymphocyte (CTL)-mediated reactions are associated with tissue transplant rejection and contact dermatitis ( [link] ). For this form of cell-mediated hypersensitivity, APCs process and present the antigen with MHC I to naïve CD8 T cells. When these naïve CD8 T cells are activated, they proliferate and differentiate into CTLs. Activated T H 1 cells can also enhance the activation of the CTLs. The activated CTLs then target and induce granzyme -mediated apoptosis in cells presenting the same antigen with MHC I. These target cells could be “self” cells that have absorbed the foreign antigen (such as with contact dermatitis due to poison ivy), or they could be transplanted tissue cells displaying foreign antigen from the donor.

a) Sensitization. Antigens from poison ivy enter dendritic cells in skin. The dendritic cell activates a T-cell which becomes a memory helper T cell. b) Immune response. Macrophages, memory helper T cells, and cytotoxic T cells produce a large lesion on the skin due to dytikine activation.
Exposure to hapten antigens in poison ivy can cause contact dermatitis, a type IV hypersensitivity. (a) The first exposure to poison ivy does not result in a reaction. However, sensitization stimulates helper T cells, leading to production of memory helper T cells that can become reactivated on future exposures. (b) Upon secondary exposure, the memory helper T cells become reactivated, producing inflammatory cytokines that stimulate macrophages and cytotoxic T cells to induce an inflammatory lesion at the exposed site. This lesion, which will persist until the allergen is removed, can inflict significant tissue damage if it continues long enough.
Type IV Hypersensitivities
Subcategory Antigen Effector Mechanism Examples
1 Soluble antigen Activated macrophages damage tissue and promote inflammatory response Contact dermatitis (e.g., exposure to latex) and delayed-type hypersensitivity (e.g., tuberculin reaction)
2 Soluble antigen Eosinophil recruitment and activation release cytokines and pro-inflammatory chemicals Chronic asthma and chronic allergic rhinitis
3 Cell-associated antigen CTL-mediated cytotoxicity Contact dermatitis (e.g., contact with poison ivy) and tissue-transplant rejection

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Source:  OpenStax, Microbiology. OpenStax CNX. Nov 01, 2016 Download for free at http://cnx.org/content/col12087/1.4
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