Purpose of review In many regions of the world, a high prevalence of HIV-1, helminthic and Mycobacterium tuberculosis (Mtb) infections can be found. Here, we summarize the types of immune responses induced and/or modulated by these pathogens and the consequences for HIV-1 disease. Recent findings Helminths predominantly induce strong T helper (Th) 2 cellular responses which are downregulated in chronic disease. The anatomical niche populated by helminths plays a key factor in the effect these parasites have on HIV-1 transmission and subsequent replication. Gut-associated helminths have been found to increase HIV-1 transmission via the lesions they provide. In spite of this, the many immune modulatory molecules secreted by the parasites may inhibit or slow HIV-1 infection. In contrast, Mtb is mainly restricted to the lung and the Mtb-specific Th cells induced are highly susceptible to HIV-1 infection and replication. Antigens from both pathogens have immunomodulatory activity that can skew cellular immune responses in specific directions. Summary The effect of helminths and Mtb on modulating immune responses is varied and complex with both their location and phenotype potentially influencing HIV-1 disease. These pathogens have evolved a complex array of molecules which have the capacity to modulate immunity and preserve pathogen survival.
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Univ Cape Town, Inst Infect Dis & Mol Med, Clin Infect Dis Res Initiat, ZA-7925 Observatory, South AfricaUniv Cape Town, Inst Infect Dis & Mol Med, Clin Infect Dis Res Initiat, ZA-7925 Observatory, South Africa
Du Bruyn, Elsa
Wilkinson, Robert John
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Univ Cape Town, Inst Infect Dis & Mol Med, Clin Infect Dis Res Initiat, ZA-7925 Observatory, South Africa
Imperial Coll London, Dept Med, London W2 1PG, England
Francis Crick Inst, Mill Hill Lab, London NW7 1AA, EnglandUniv Cape Town, Inst Infect Dis & Mol Med, Clin Infect Dis Res Initiat, ZA-7925 Observatory, South Africa
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Univ Michigan, Dept Math, Ann Arbor, MI 48109 USA
Los Alamos Natl Lab, Div Theoret, Los Alamos, NM 87545 USAUniv Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Bauer, Amy L.
Hogue, Ian B.
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Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Hogue, Ian B.
Marino, Simeone
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Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
Marino, Simeone
Kirschner, Denise E.
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Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
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Univ London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept Immunol, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept Immunol, London SW10 9NH, England
Westrop, S. J.
Jackson, A.
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Univ London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept HIV GU Med, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept Immunol, London SW10 9NH, England
Jackson, A.
Gazzard, B.
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Univ London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept HIV GU Med, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept Immunol, London SW10 9NH, England
Gazzard, B.
Imami, N.
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Univ London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept Immunol, London SW10 9NH, EnglandUniv London Imperial Coll Sci Technol & Med, Chelsea & Westminster Hosp, Dept Immunol, London SW10 9NH, England