THE IN-VITRO INDUCTION OF HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) REPLICATION IN PURIFIED PROTEIN DERIVATIVE-POSITIVE HIV-INFECTED PERSONS BY RECALL ANTIGEN RESPONSE TO MYCOBACTERIUM-TUBERCULOSIS IS THE RESULT OF ABALANCE OF THE EFFECTS OF ENDOGENOUS INTERLEUKIN-2 AND PROINFLAMMATORY AND ANTIINFLAMMATORY CYTOKINES
D. Goletti et al., THE IN-VITRO INDUCTION OF HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) REPLICATION IN PURIFIED PROTEIN DERIVATIVE-POSITIVE HIV-INFECTED PERSONS BY RECALL ANTIGEN RESPONSE TO MYCOBACTERIUM-TUBERCULOSIS IS THE RESULT OF ABALANCE OF THE EFFECTS OF ENDOGENOUS INTERLEUKIN-2 AND PROINFLAMMATORY AND ANTIINFLAMMATORY CYTOKINES, The Journal of infectious diseases, 177(5), 1998, pp. 1332-1338
Coinfection with Mycobacterium tuberculosis and human immunodeficiency
virus (HIV) is a serious problem, particularly in developing countrie
s. Recently, M. tuberculosis and purified protein derivative (PPD) wer
e demonstrated to induce HIV replication in CD8 T cell-depleted periph
eral blood mononuclear cells from HIV-positive, PPD-positive persons b
ut not in cells from PPD-negative persons. The role of endogenous and
exogenous cytokines in modulating M. tuberculosis-induced HIV replicat
ion was evaluated. M. tuberculosis-induced HIV replication decreased f
ollowing simultaneous inhibition of endogenous interleukin (IL)-2, IL-
1 beta, and tumor necrosis factor-alpha by the addition of soluble rec
eptors and receptor antagonists or following exogenous IL-10 and trans
forming growth factor (TGF)-beta. In contrast, neutralization of endog
enous IL-10 and TGF-beta augmented M. tuberculosis-induced HIV replica
tion by increasing cellular activation. Thus, the balance between IL-2
and proinflammatory and antiinflammatory cytokines plays a major role
in,II. tuberculosis-induced replication of HIV.