Increased plasma levels of soluble ICAM-1 and ELAM-1 (E-selectin) during acute Plasmodium falciparum malaria

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Increased plasma levels of soluble ICAM-1 and ELAM-1 (E-selectin) during acute Plasmodium falciparum malaria. / Hviid, L; Theander, T G; Elhassan, I M; Jensen, J B.

In: Immunology Letters, Vol. 36, No. 1, 1993, p. 51-8.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hviid, L, Theander, TG, Elhassan, IM & Jensen, JB 1993, 'Increased plasma levels of soluble ICAM-1 and ELAM-1 (E-selectin) during acute Plasmodium falciparum malaria', Immunology Letters, vol. 36, no. 1, pp. 51-8. https://doi.org/10.1016/0165-2478%2893%2990068-D

APA

Hviid, L., Theander, T. G., Elhassan, I. M., & Jensen, J. B. (1993). Increased plasma levels of soluble ICAM-1 and ELAM-1 (E-selectin) during acute Plasmodium falciparum malaria. Immunology Letters, 36(1), 51-8. https://doi.org/10.1016/0165-2478%2893%2990068-D

Vancouver

Hviid L, Theander TG, Elhassan IM, Jensen JB. Increased plasma levels of soluble ICAM-1 and ELAM-1 (E-selectin) during acute Plasmodium falciparum malaria. Immunology Letters. 1993;36(1):51-8. https://doi.org/10.1016/0165-2478%2893%2990068-D

Author

Hviid, L ; Theander, T G ; Elhassan, I M ; Jensen, J B. / Increased plasma levels of soluble ICAM-1 and ELAM-1 (E-selectin) during acute Plasmodium falciparum malaria. In: Immunology Letters. 1993 ; Vol. 36, No. 1. pp. 51-8.

Bibtex

@article{6e66e000a07011dd86a6000ea68e967b,
title = "Increased plasma levels of soluble ICAM-1 and ELAM-1 (E-selectin) during acute Plasmodium falciparum malaria",
abstract = "Acute P. falciparum malaria is associated with a loss of antigen-responsiveness of peripheral T cells, depletion of T cells characterized by high surface expression of the adhesion molecule LFA-1, and increased plasma levels of the T-cell activation marker soluble IL-2 receptor (sIL-2R). In the present study we show that clinical episodes of P. falciparum malaria produced an increase in plasma levels of soluble ICAM-1 (sICAM-1) and ELAM-1 (sELAM-1). The increase was transient and subsided slowly (sICAM-1) or rapidly (sELAM-1) following drug cure. The increases in plasma sICAM-1 and sELAM-1 were significantly correlated, and were furthermore associated with a concomitant increase in plasma levels of sIL-2R. Finally, plasma levels of sICAM-1, but not sELAM-1, were inversely correlated to the fraction of peripheral T cells having high surface expression of LFA-1, the receptor for T-cell adhesion to ICAM-1. Taken together, these observations suggest that acute P. falciparum malaria is characterized by a state of endothelial inflammation associated with the adherence of activated T cells.",
author = "L Hviid and Theander, {T G} and Elhassan, {I M} and Jensen, {J B}",
note = "Keywords: Acute Disease; Cell Adhesion; Cell Adhesion Molecules; E-Selectin; Enzyme-Linked Immunosorbent Assay; Humans; Intercellular Adhesion Molecule-1; Lymphocyte Activation; Malaria, Falciparum; Receptors, Interleukin-2; Solubility; T-Lymphocytes",
year = "1993",
doi = "10.1016/0165-2478%2893%2990068-D",
language = "English",
volume = "36",
pages = "51--8",
journal = "Immunology Letters",
issn = "0165-2478",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Increased plasma levels of soluble ICAM-1 and ELAM-1 (E-selectin) during acute Plasmodium falciparum malaria

AU - Hviid, L

AU - Theander, T G

AU - Elhassan, I M

AU - Jensen, J B

N1 - Keywords: Acute Disease; Cell Adhesion; Cell Adhesion Molecules; E-Selectin; Enzyme-Linked Immunosorbent Assay; Humans; Intercellular Adhesion Molecule-1; Lymphocyte Activation; Malaria, Falciparum; Receptors, Interleukin-2; Solubility; T-Lymphocytes

PY - 1993

Y1 - 1993

N2 - Acute P. falciparum malaria is associated with a loss of antigen-responsiveness of peripheral T cells, depletion of T cells characterized by high surface expression of the adhesion molecule LFA-1, and increased plasma levels of the T-cell activation marker soluble IL-2 receptor (sIL-2R). In the present study we show that clinical episodes of P. falciparum malaria produced an increase in plasma levels of soluble ICAM-1 (sICAM-1) and ELAM-1 (sELAM-1). The increase was transient and subsided slowly (sICAM-1) or rapidly (sELAM-1) following drug cure. The increases in plasma sICAM-1 and sELAM-1 were significantly correlated, and were furthermore associated with a concomitant increase in plasma levels of sIL-2R. Finally, plasma levels of sICAM-1, but not sELAM-1, were inversely correlated to the fraction of peripheral T cells having high surface expression of LFA-1, the receptor for T-cell adhesion to ICAM-1. Taken together, these observations suggest that acute P. falciparum malaria is characterized by a state of endothelial inflammation associated with the adherence of activated T cells.

AB - Acute P. falciparum malaria is associated with a loss of antigen-responsiveness of peripheral T cells, depletion of T cells characterized by high surface expression of the adhesion molecule LFA-1, and increased plasma levels of the T-cell activation marker soluble IL-2 receptor (sIL-2R). In the present study we show that clinical episodes of P. falciparum malaria produced an increase in plasma levels of soluble ICAM-1 (sICAM-1) and ELAM-1 (sELAM-1). The increase was transient and subsided slowly (sICAM-1) or rapidly (sELAM-1) following drug cure. The increases in plasma sICAM-1 and sELAM-1 were significantly correlated, and were furthermore associated with a concomitant increase in plasma levels of sIL-2R. Finally, plasma levels of sICAM-1, but not sELAM-1, were inversely correlated to the fraction of peripheral T cells having high surface expression of LFA-1, the receptor for T-cell adhesion to ICAM-1. Taken together, these observations suggest that acute P. falciparum malaria is characterized by a state of endothelial inflammation associated with the adherence of activated T cells.

U2 - 10.1016/0165-2478%2893%2990068-D

DO - 10.1016/0165-2478%2893%2990068-D

M3 - Journal article

C2 - 7688346

VL - 36

SP - 51

EP - 58

JO - Immunology Letters

JF - Immunology Letters

SN - 0165-2478

IS - 1

ER -

ID: 6748382