TY - JOUR
T1 - Naturally exposed populations differ in their T1 and T2 responses to the circumsporozoite protein of Plasmodium falciparum
AU - Reece, W. H H
AU - Plebanski, M.
AU - Akinwunmi, P.
AU - Gothard, P.
AU - Flanagan, K. L.
AU - Lee, E. A M
AU - Cortina-Borja, M.
AU - Hill, A. V S
AU - Pinder, M.
PY - 2002
Y1 - 2002
N2 - T-cell responses directed against the circumsporozoite protein (CS) of Plasmodium falciparum can mediate protection against malaria. We determined the frequency of T cells reactive to different regions of the CS in the blood of donors naturally exposed to P. falciparum by examining TI (gamma interferon [IFN-γ] ELISPOT assay), T2 (interleukin 4 [IL-4] ELISPOT assay), and proliferative T-cell responses. The proliferative responses were weak, which confirmed previous observations. The responses to the CS in the IL-4 and IFN-γ ELISPOT assays were also weak (6 cells), much weaker than the response to the purified protein derivative of Mycobacterium tuberculosis in the same donors. Moreover, a response in one assay could not be used to predict a response in either of the other assays, suggesting that although these assays may measure different responding cells, all of the responses are weakly induced by natural exposure. Interestingly, the two different study populations used had significantly different T1 and T2 biases in their responses in the C terminus of the protein, suggesting that the extent of P. falciparum exposure can affect regulation of the immune system.
AB - T-cell responses directed against the circumsporozoite protein (CS) of Plasmodium falciparum can mediate protection against malaria. We determined the frequency of T cells reactive to different regions of the CS in the blood of donors naturally exposed to P. falciparum by examining TI (gamma interferon [IFN-γ] ELISPOT assay), T2 (interleukin 4 [IL-4] ELISPOT assay), and proliferative T-cell responses. The proliferative responses were weak, which confirmed previous observations. The responses to the CS in the IL-4 and IFN-γ ELISPOT assays were also weak (6 cells), much weaker than the response to the purified protein derivative of Mycobacterium tuberculosis in the same donors. Moreover, a response in one assay could not be used to predict a response in either of the other assays, suggesting that although these assays may measure different responding cells, all of the responses are weakly induced by natural exposure. Interestingly, the two different study populations used had significantly different T1 and T2 biases in their responses in the C terminus of the protein, suggesting that the extent of P. falciparum exposure can affect regulation of the immune system.
UR - http://www.scopus.com/inward/record.url?scp=0036182404&partnerID=8YFLogxK
U2 - 10.1128/IAI.70.3.1468-1474.2002
DO - 10.1128/IAI.70.3.1468-1474.2002
M3 - Article
C2 - 11854234
AN - SCOPUS:0036182404
SN - 0019-9567
VL - 70
SP - 1468
EP - 1474
JO - Infection and Immunity
JF - Infection and Immunity
IS - 3
ER -