Publication | Closed Access
Inhibition of HIV-1 Infection by the b-Chemokine MDC
177
Citations
4
References
2016
Year
Unknown Venue
Adaptive Immune SystemImmunologyImmune RegulationImmunodominanceCd8 TCd4 T Cell ResponsesSoluble ActivityAntiviral DrugImmune SystemHuman RetrovirusAntiviral Drug DevelopmentTumor ImmunityImmune SurveillanceT Cell ImmunityChronic Viral InfectionHivIsolate Hiv-1iiibCell BiologyAids PathogenesisAntiviral ResponseHiv-1 InfectionCellular Immune ResponseMedicineViral ImmunityDrug Discovery
CD8 T lymphocytes from individuals infected with human immunodeficiency virus–type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A protein associated with this activity was purified from the culture supernatant of an immortalized CD8 T cell clone and identified as the b-chemokine macrophage-derived chemokine (MDC). MDC suppressed infection of CD8 cell–depleted peripheral blood mononuclear cells by primary non–syncytium-inducing and syncytium-inducing isolates of HIV-1 and the T cell line–adapted isolate HIV-1IIIB. MDC was expressed in activated, but not resting, peripheral blood mononuclear cells and binds a receptor on activated primary T cells. These observations indicate that b-chemokines are responsible for a major proportion of HIV-1–specific suppressor activity produced by primary T cells.
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