Malaria and pregnancy in Cameroonian primigravidae: humoral and cellular immune responses to Plasmodium falciparum blood-stage antigens.

To investigate the mechanisms underlying the increased susceptibility to malaria in pregnant women, we determined the level of malaria-specific immunity in primigravidae. Humoral and cellular in vitro responses to unpurified (a crude schizont extract and a gametocyte preparation) and purified (affinity-purified Pf155/ring-infected erythrocyte surface antigen [RESA]) Plasmodium falciparum proteins, an immunodominant 45/47-kilodalton antigen from Mycobacterium bovis, and leucoagglutinin were compared between 52 primigravidae and 52 nonpregnant women from a semirural area of Cameroon. In vitro cellular responses were investigated in terms of lymphocyte proliferation, as well as production of interleukin-2 (IL-2), interferon-gamma (IFN-gamma), and IL-4. Cells from primigravidae exhibited a reduced proliferative response to schizont and gametocyte antigens, as well as to the M. bovis antigen. Conversely, the IL-2 response to Pf155/RESA was reduced. Interleukin-4 and IFN-gamma production did not appear to be affected in primigravidae. Antibody levels were also similar between pregnant and nonpregnant women. Our results underline the importance of examining several parameters of T cell activation with different types of antigens for a correct evaluation of the ability of lymphocytes to respond to malaria.

[1]  J. L. Le Hesran,et al.  Increase of birth weight following chloroquine chemoprophylaxis during the first pregnancy: results of a randomized trial in Cameroon. , 1995, The American journal of tropical medicine and hygiene.

[2]  P. Kourilsky,et al.  Differential cytokine expression in maternal blood and placenta during murine gestation. , 1994, Journal of immunology.

[3]  T. Mosmann,et al.  Synthesis of T helper 2-type cytokines at the maternal-fetal interface. , 1993, Journal of immunology.

[4]  T. Olsson,et al.  Number of interleukin‐4‐ and interferon‐γ‐secreting human T cells reactive with tetanus toxoid and the mycobacterial antigen PPD or phytohemagglutinin: distinct response profiles depending on the type of antigen used for activation , 1993, European journal of immunology.

[5]  A. Holder,et al.  A longitudinal study of naturally acquired cellular and humoral immune responses to a merozoite surface protein (MSP1) of Plasmodium falciparum in an area of seasonal malaria transmission , 1993, Parasite immunology.

[6]  T. Mosmann,et al.  Bidirectional cytokine interactions in the maternal-fetal relationship: is successful pregnancy a TH2 phenomenon? , 1993, Immunology today.

[7]  P. Pescher,et al.  Isolation of a proline-rich mycobacterial protein eliciting delayed-type hypersensitivity reactions only in guinea pigs immunized with living mycobacteria. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[8]  C. Chougnet,et al.  Human immune responses to the Plasmodium falciparum ring-infected erythrocyte surface antigen (Pf155/RESA) after a decrease in malaria transmission in Madagascar. , 1993, The American journal of tropical medicine and hygiene.

[9]  C. Menéndez,et al.  Suppressed peripheral and placental blood lymphoproliferative responses in first pregnancies: relevance to malaria. , 1993, The American journal of tropical medicine and hygiene.

[10]  C. C. Campbell,et al.  Malaria and pregnancy in Cameroonian women. Naturally acquired antibody responses to asexual blood-stage antigens and the circumsporozoite protein of Plasmodium falciparum. , 1992, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[11]  S. Romagnani Human TH1 and TH2 subsets: doubt no more. , 1991, Immunology today.

[12]  M. Clerici,et al.  Early T-helper cell defects in HIV infection. , 1991, AIDS.

[13]  J. Grassi,et al.  Determination of ILlα, ILlβ and IL2 in Biological Media using Specific Enzyme Immunometric Assays , 1991, Immunological reviews.

[14]  C. Chougnet,et al.  Longitudinal study of the cellular response to Pf155/RESA and circumsporozoite protein in Madagascar. , 1990, Immunology letters.

[15]  T. Mosmann,et al.  Heterogeneity of mouse helper T cells. Evidence from bulk cultures and limiting dilution cloning for precursors of Th1 and Th2 cells. , 1990, Journal of immunology.

[16]  A. Weinberg,et al.  CD4+ T cell subsets. Lymphokine secretion of memory cells and of effector cells that develop from precursors in vitro. , 1990, Journal of immunology.

[17]  J. Grassi,et al.  Production of monoclonal antibodies against interleukin-1α and -1β: Development of two enzyme immunometric assays (EIA) using acetylcholinesterase and their application to biological media , 1989 .

[18]  B. Greenwood,et al.  Suppression of cell-mediated immune responses to malaria antigens in pregnant Gambian women. , 1989, The American journal of tropical medicine and hygiene.

[19]  E. Weinberg Pregnancy-associated depression of cell-mediated immunity. , 1984, Reviews of infectious diseases.

[20]  I. McGregor Epidemiology, malaria and pregnancy. , 1984, The American journal of tropical medicine and hygiene.

[21]  M. Wahlgren,et al.  Antibodies in malarial sera to parasite antigens in the membrane of erythrocytes infected with early asexual stages of Plasmodium falciparum , 1984, The Journal of experimental medicine.

[22]  S. Birkeland,et al.  Lymphocyte Transformation with Mitogens and Antigens during Normal Human Pregnancy: a Longitudinal Study , 1980, Scandinavian journal of immunology.

[23]  W. Straube,et al.  [Immunobiology of pregnancy]. , 1974, Zentralblatt fur Gynakologie.

[24]  R. Steketee,et al.  Serological reactivity to the ring-infected erythrocyte surface antigen and circumsporozoite protein in gravid and nulligravid women infected with Plasmodium falciparum. , 1989, Transactions of the Royal Society of Tropical Medicine and Hygiene.

[25]  B. Brabin An analysis of malaria in pregnancy in Africa. , 1983, Bulletin of the World Health Organization.