首页> 美国卫生研究院文献>Infection and Immunity >Cellular and humoral immune responses to well-defined blood stage antigens (major merozoite surface antigen) of Plasmodium falciparum in adults from an Indian zone where malaria is endemic.
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Cellular and humoral immune responses to well-defined blood stage antigens (major merozoite surface antigen) of Plasmodium falciparum in adults from an Indian zone where malaria is endemic.

机译:来自印度疟疾流行地区成人中恶性疟原虫的明确血液阶段抗原(主要裂殖子表面抗原)的细胞和体液免疫反应。

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摘要

Conserved and variant regions of two blood stage vaccine candidate antigens of Plasmodium falciparum, merozoite surface antigen (MSA-1) and ring-infected erythrocyte surface antigen (Pf155/RESA), have been shown to be immunogenic. However, the relative immunogenicity of these immunogens in different populations has not been studied. The conserved N-terminal region of MSA-1 was investigated for its immunogenicity by studying cellular (T cell) and humoral (B cell) immune responses in P. falciparum-primed individuals, living in malaria-hyperendemic areas (Orissa State, India), where malaria presents an alarming situation. MSA-1-derived synthetic peptides contained sequences that activated T cells to proliferate and release gamma interferon in vitro. There was considerable variation in the responses to different peptides. However, the highest responses (51% [18 of 35] by proliferation and 34% [12 of 35] by gamma interferon release) were obtained with a synthetic hybrid peptide containing sequences from conserved N- and C-terminal repeat regions of MSA-1 and Pf155/RESA, respectively. Antibody reactivities in an enzyme immunoassay of plasma samples from these donors to different peptides used for T-cell activation were heterogeneous. In general, there was poor correlation between DNA synthesis and either gamma interferon release or antibody responses in individual donors, underlining the importance of examining several parameters of T-cell activation to assess the total T-cell responsiveness of a study population to a given antigen. However, the results from our studies suggest that synthetic constructs containing sequences from the N- and C-terminal regions of MSA-1 and Pf155/RESA representing different erythrocytic stages of the P. falciparum parasite are more immunogenic in humans living in malaria-hyperendemic areas of India who have been primed by natural infection.
机译:恶性疟原虫的两种血液阶段疫苗候选抗原,裂殖子表面抗原(MSA-1)和环感染的红细胞表面抗原(Pf155 / RESA)的保守区和变异区已显示具有免疫原性。但是,尚未研究这些免疫原在不同人群中的相对免疫原性。通过研究生活在疟疾高流行地区(印度奥里萨邦)的恶性疟原虫引发的个体的细胞(T细胞)和体液(B细胞)免疫应答,研究了MSA-1保守的N末端区域的免疫原性。 ,那里的疟疾令人震惊。 MSA-1衍生的合成肽包含激活T细胞以在体外增殖和释放γ干扰素的序列。对不同肽的反应有相当大的差异。但是,使用合成杂合肽可获得最高响应(通过增殖,占51%[35分之18],通过γ干扰素释放34%[35分之12]),该杂合肽含有来自MSA-保守N和C端重复区域的序列1和Pf155 / RESA。在来自这些供体的血浆样品的酶免疫测定中,用于T细胞活化的不同肽的抗体反应性是异质的。一般而言,单个供体中DNA合成与γ干扰素释放或抗体反应之间的相关性较差,强调了检查T细胞活化的几个参数以评估研究人群对特定抗原的总T细胞反应性的重要性。 。但是,我们的研究结果表明,含有恶性疟原虫不同红细胞阶段代表MSA-1和Pf155 / RESA N-和C-末端区域的序列的合成构建体在生活在疟疾-高血统人群中具有更高的免疫原性印度的自然感染引发的地区。

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