The Antibody-Secreting Cell Response to infection: Kinetics and Clinical Applications

被引:54
作者
Carter, Michael J. [1 ]
Mitchell, Ruth M. [1 ]
Sauteur, Patrick M. Meyer [2 ]
Kelly, Dominic F. [1 ]
Trueck, Johannes [1 ,2 ]
机构
[1] Univ Oxford, Oxford Vaccine Grp, Dept Paediat, NIHR Oxford Biomed Res Ctr, Oxford, England
[2] Univ Childrens Hosp, Zurich, Switzerland
基金
英国惠康基金;
关键词
B cells; antibody-secreting cells; plasmablasts; adaptive immunity; diagnosis; transcriptomics; monoclonal antibodies; B cell receptor sequencing; DENGUE VIRUS-INFECTION; MEMORY B-CELL; LYMPHOCYTE SUPERNATANT ALS; GENE TRANSCRIPT ABUNDANCE; MUCOSAL IMMUNE-RESPONSES; STREPTOCOCCUS-PNEUMONIAE; PERIPHERAL-BLOOD; MYCOBACTERIUM-TUBERCULOSIS; NEUTRALIZING ANTIBODIES; REPERTOIRE DYNAMICS;
D O I
10.3389/fimmu.2017.00630
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite the availability of advances in molecular diagnostic testing for infectious disease, there is still a need for tools that advance clinical care and public health. Current methods focus on pathogen detection with unprecedented precision, but often lack specificity. In contrast, the host immune response is highly specific for the infecting pathogen. Serological studies are rarely helpful in clinical settings, as they require acute and convalescent antibody testing. However, the B cell response is much more rapid and short-lived, making it an optimal target for determining disease aetiology in patients with infections. The performance of tests that aim to detect circulating antigen-specific antibody-secreting cells (ASCs) has previously been unclear. Test performance is reliant on detecting the presence of ASCs in the peripheral blood. As such, the kinetics of the ASC response to infection, the antigen specificity of the ASC response, and the methods of ASC detection are all critical. In this review, we summarize previous studies that have used techniques to enumerate ASCs during infection. We describe the emergence, peak, and waning of these cells in peripheral blood during infection with a number of bacterial and viral pathogens, as well as malaria infection. We find that the timing of antigen-specific ASC appearance and disappearance is highly conserved across pathogens, with a peak response between day 7 and day 8 of illness and largely absent following day 14 since onset of symptoms. Data show a sensitivity of similar to 90% and specificity >80% for pathogen detection using ASC-based methods. Overall, the summarised work indicates that ASC-based methods may be very sensitive and highly specific for determining the etiology of infection and have some advantages over current methods. Important areas of research remain, including more accurate definition of the timing of the ASC response to infection, the biological mechanisms underlying variability in its magnitude and the evolution and the B cell receptor in response to immune challenge. Nonetheless, there is potential of the ASC response to infection to be exploited as the basis for novel diagnostic tests to inform clinical care and public health priorities.
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