Journal Article10.1146/ANNUREV.IMMUNOL.19.1.93
Immunology of tuberculosis.
JoAnne L. Flynn,John W. Y. Chan +1 more
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TL;DR: This review summarizes the current understanding of the host immune response, with emphasis on the roles of macrophages, T cells, and the cytokine/chemokine network in engendering protective immunity.
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Abstract: The resurgence of tuberculosis worldwide has intensified research efforts directed at examining the host defense and pathogenic mechanisms operative in Mycobacterium tuberculosis infection. This review summarizes our current understanding of the host immune response, with emphasis on the roles of macrophages, T cells, and the cytokine/chemokine network in engendering protective immunity. Specifically, we summarize studies addressing the ability of the organism to survive within macrophages by controlling phagolysosome fusion. The recent studies on Toll-like receptors and the impact on the innate response to M. tuberculosis are discussed. We also focus on the induction, specificity, and effector functions of CD4(+) and CD8(+) T cells, and the roles of cytokines and chemokines in the induction and effector functions of the immune response. Presentation of mycobacterial antigens by MHC class I, class II, and CD1 as well as the implications of these molecules sampling various compartments of the cell for presentation to T cells are discussed. Increased attention to this disease and the integration of animal models and human studies have afforded us a greater understanding of tuberculosis and the steps necessary to combat this infection. The pace of this research must be maintained if we are to realize an effective vaccine in the next decades.
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References
Macrophage differentiation marker MyD88 is a member of the Toll/IL-1 receptor family.
TL;DR: It is demonstrated that the open reading frame of MyD88, a gene induced in myeloid differentiation, is related to the cytoplasmic domains of the interleukin-1 receptor and the Toll gene product.
Killing of Mycobacterium microti by immunologically activated macrophages
Linda L. Walker,D. B. Lowrie +1 more
TL;DR: It is reported here that normal mouse peritoneal macrophages can be activated in vitro by lymphokines to kill Mycobacterium microti, the natural agent of tuberculosis in voles, and that added catalase protects the bacilli from killing.
Adoptive protection of the Mycobacterium tuberculosis-infected lung: Dissociation between cells that passively transfer protective immunity and those that transfer delayed-type hypersensitivity to tuberculin
Ian M. Orme,Frank M. Collins +1 more
TL;DR: It is indicated, that DTH and protective anti-tuberculous immunity are dissociable phenomena, mediated by separate populations of T lymphocytes.
•Journal Article
Activation of macrophages to inhibit proliferation of mycobacterium-tuberculosis - comparison of the effects of recombinant gamma-interferon on human-monocytes and murine peritoneal-macrophages
TL;DR: Human monocytes from seven donors were not on average significantly different from non-activated murine peritoneal cells in their ability to inhibit BCG and, when calculated relative to growth of bacilli in the same medium without macrophages, to enhance the growth of Mycobacterium tuberculosis.
Dichotomy of cytokine profiles in patients and high-risk healthy subjects exposed to tuberculosis.
TL;DR: The elevated levels of IL-4+CD4+ T cells seen in patients may contribute to the downregulation of IFN-γ expression and the crucial effector function of CD4 T cells, leading to the persistence of disease and the immunopathology characteristically seen in Patients.
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