Detection of cytotoxic T lymphocytes specific for synthetic peptides of gp160 in HIV-seropositive individuals

التفاصيل البيبلوغرافية
العنوان: Detection of cytotoxic T lymphocytes specific for synthetic peptides of gp160 in HIV-seropositive individuals
المؤلفون: M Clerici, D R Lucey, R A Zajac, R N Boswell, H M Gebel, H Takahashi, J A Berzofsky, G M Shearer
المصدر: The Journal of Immunology. 146:2214-2219
بيانات النشر: The American Association of Immunologists, 1991.
سنة النشر: 1991
مصطلحات موضوعية: Immunology, Immunology and Allergy
الوصف: Four synthetic peptides corresponding to the IIIB sequence of gp160 of HIV were recently reported to stimulate Th cell function by PBL from HIV-infected, asymptomatic patients. In the present report, we used these same peptides to demonstrate CTL activity in a similar patient population. EBV-transformed B-cell lines from asymptomatic, HIV seropositive and seronegative control donors were pre-incubated with the peptides. Fresh PBL from 19 (76%) of 25 HIV seropositive donors lysed autologous targets pulsed with at least one of the four peptides. Autologous targets pulsed with two non-immunogenic peptides were not lysed. PBL from none of the eight HIV seronegative controls lysed peptide-preincubated autologous targets. The CTL activity was mediated by T cells, was predominantly MHC class I restricted, and was increased by in vitro restimulation of PBL with the peptides. HLA A-2 was identified as a restricting element for all four peptides in different patients, and for three of the peptides in the same donor. HLA-A1 or -B8 may also present some of the peptides. Thus, the same peptides can be recognized by human Th cells and class I MHC-restricted CTL.
تدمد: 1550-6606
0022-1767
DOI: 10.4049/jimmunol.146.7.2214
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0807cca666e106aadd58dc161185ecac
https://doi.org/10.4049/jimmunol.146.7.2214
رقم الانضمام: edsair.doi...........0807cca666e106aadd58dc161185ecac
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15506606
00221767
DOI:10.4049/jimmunol.146.7.2214