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Cellular anti-GP120 cytolytic reactivities in HIV-1 seropositive individuals.
- Source :
-
Lancet (London, England) [Lancet] 1988 Apr 23; Vol. 1 (8591), pp. 902-5. - Publication Year :
- 1988
-
Abstract
- Forty-one patients seropositive for human immunodeficiency virus type 1 (HIV-1) were assessed for cell-mediated cytotoxicity (CMC) against autologous target cells bearing the major envelope glycoprotein of HIV-1, gp120. Effector lymphocytes from over 85% of seropositive patients showed CMC specific for gp120-coated targets, whereas seronegative individuals had no detectable CMC. As a group, symptomless individuals had the highest levels of CMC; patients with AIDS-related complex and AIDS showed progressively diminished reactivity. The gp120-specific CMC was mediated by a population of non-T-cell effectors phenotypically resembling NK/K cells. Cytolysis was not restricted by major histocompatibility complex determinants, as shown by killing of heterologous gp120-adsorbed targets and of HIV-1-infected cell-lines. Gp120-specific CMC was highly augmented in the presence of interleukin 2, so it may be possible to develop therapeutic strategies aimed at destruction of virus-producing cell reservoirs in infected individuals through stimulation of HIV-specific host CMC.
- Subjects :
- Antibodies, Monoclonal analysis
HIV Antibodies
HIV Envelope Protein gp120
Humans
Interleukin-2 pharmacokinetics
Killer Cells, Natural drug effects
Phenotype
Recombinant Proteins pharmacokinetics
Retroviridae Proteins pharmacokinetics
Stimulation, Chemical
T-Lymphocytes immunology
T-Lymphocytes metabolism
Viral Envelope Proteins metabolism
Viral Envelope Proteins pharmacokinetics
Antibodies, Viral analysis
Antibody-Dependent Cell Cytotoxicity drug effects
Deltaretrovirus immunology
HIV Seropositivity immunology
Retroviridae Proteins immunology
Viral Envelope Proteins immunology
Subjects
Details
- Language :
- English
- ISSN :
- 0140-6736
- Volume :
- 1
- Issue :
- 8591
- Database :
- MEDLINE
- Journal :
- Lancet (London, England)
- Publication Type :
- Academic Journal
- Accession number :
- 2895830
- Full Text :
- https://doi.org/10.1016/s0140-6736(88)91713-8