Recognition of Leishmania antigens by T lymphocytes from nonexposed individuals

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Recognition of Leishmania antigens by T lymphocytes from nonexposed individuals. / Kemp, M; Hansen, M B; Theander, T G.

In: Infection and Immunity, Vol. 60, No. 6, 1992, p. 2246-51.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kemp, M, Hansen, MB & Theander, TG 1992, 'Recognition of Leishmania antigens by T lymphocytes from nonexposed individuals', Infection and Immunity, vol. 60, no. 6, pp. 2246-51.

APA

Kemp, M., Hansen, M. B., & Theander, T. G. (1992). Recognition of Leishmania antigens by T lymphocytes from nonexposed individuals. Infection and Immunity, 60(6), 2246-51.

Vancouver

Kemp M, Hansen MB, Theander TG. Recognition of Leishmania antigens by T lymphocytes from nonexposed individuals. Infection and Immunity. 1992;60(6):2246-51.

Author

Kemp, M ; Hansen, M B ; Theander, T G. / Recognition of Leishmania antigens by T lymphocytes from nonexposed individuals. In: Infection and Immunity. 1992 ; Vol. 60, No. 6. pp. 2246-51.

Bibtex

@article{7c585a70a0db11dd86a6000ea68e967b,
title = "Recognition of Leishmania antigens by T lymphocytes from nonexposed individuals",
abstract = "Crude antigen preparations of Leishmania promastigote sonicates were found to induce in vitro proliferation and gamma interferon production in peripheral blood mononuclear cells (PBMC) from individuals without known exposure to the parasite. The proliferating cells were mainly CD2-positive T cells. The proliferative response was maximal after more than 6 days of incubation with the antigens in contrast to the proliferation induced by the mitogenic lectin phytohemagglutinin (PHA), which peaked after 3 to 5 days. Judged by limiting dilution analysis, the frequencies of antigen-reactive precursor cells were less than 1:10,000 and varied considerably between individuals. Depletion of CD45R0-positive (memory) cells from the PBMC abolished proliferative responses induced by Leishmania antigen and by tetanus toxoid. In cell populations depleted of CD45RA-positive (naive) cells, only a small reduction in response was observed. Cell populations depleted of either CD45R0-positive cells or CD45RA-positive cells both responded to PHA. We conclude that presumably unexposed individuals have a low number of Leishmania-reactive T cells in their circulatory systems. The Leishmania-reactive T cells in these individuals are most likely memory cells recognizing antigens present both in the Leishmania preparations and in the environment.",
author = "M Kemp and Hansen, {M B} and Theander, {T G}",
note = "Keywords: Adult; Animals; Antigens, CD; Antigens, CD45; Antigens, Protozoan; DNA; Histocompatibility Antigens; Humans; Interferon Type II; Leishmania; Lymphocyte Activation; Phenotype; T-Lymphocytes",
year = "1992",
language = "English",
volume = "60",
pages = "2246--51",
journal = "Infection and Immunity",
issn = "0019-9567",
publisher = "American Society for Microbiology",
number = "6",

}

RIS

TY - JOUR

T1 - Recognition of Leishmania antigens by T lymphocytes from nonexposed individuals

AU - Kemp, M

AU - Hansen, M B

AU - Theander, T G

N1 - Keywords: Adult; Animals; Antigens, CD; Antigens, CD45; Antigens, Protozoan; DNA; Histocompatibility Antigens; Humans; Interferon Type II; Leishmania; Lymphocyte Activation; Phenotype; T-Lymphocytes

PY - 1992

Y1 - 1992

N2 - Crude antigen preparations of Leishmania promastigote sonicates were found to induce in vitro proliferation and gamma interferon production in peripheral blood mononuclear cells (PBMC) from individuals without known exposure to the parasite. The proliferating cells were mainly CD2-positive T cells. The proliferative response was maximal after more than 6 days of incubation with the antigens in contrast to the proliferation induced by the mitogenic lectin phytohemagglutinin (PHA), which peaked after 3 to 5 days. Judged by limiting dilution analysis, the frequencies of antigen-reactive precursor cells were less than 1:10,000 and varied considerably between individuals. Depletion of CD45R0-positive (memory) cells from the PBMC abolished proliferative responses induced by Leishmania antigen and by tetanus toxoid. In cell populations depleted of CD45RA-positive (naive) cells, only a small reduction in response was observed. Cell populations depleted of either CD45R0-positive cells or CD45RA-positive cells both responded to PHA. We conclude that presumably unexposed individuals have a low number of Leishmania-reactive T cells in their circulatory systems. The Leishmania-reactive T cells in these individuals are most likely memory cells recognizing antigens present both in the Leishmania preparations and in the environment.

AB - Crude antigen preparations of Leishmania promastigote sonicates were found to induce in vitro proliferation and gamma interferon production in peripheral blood mononuclear cells (PBMC) from individuals without known exposure to the parasite. The proliferating cells were mainly CD2-positive T cells. The proliferative response was maximal after more than 6 days of incubation with the antigens in contrast to the proliferation induced by the mitogenic lectin phytohemagglutinin (PHA), which peaked after 3 to 5 days. Judged by limiting dilution analysis, the frequencies of antigen-reactive precursor cells were less than 1:10,000 and varied considerably between individuals. Depletion of CD45R0-positive (memory) cells from the PBMC abolished proliferative responses induced by Leishmania antigen and by tetanus toxoid. In cell populations depleted of CD45RA-positive (naive) cells, only a small reduction in response was observed. Cell populations depleted of either CD45R0-positive cells or CD45RA-positive cells both responded to PHA. We conclude that presumably unexposed individuals have a low number of Leishmania-reactive T cells in their circulatory systems. The Leishmania-reactive T cells in these individuals are most likely memory cells recognizing antigens present both in the Leishmania preparations and in the environment.

M3 - Journal article

C2 - 1534072

VL - 60

SP - 2246

EP - 2251

JO - Infection and Immunity

JF - Infection and Immunity

SN - 0019-9567

IS - 6

ER -

ID: 6766865