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Polyclonal B cell activation in infections: infectious agents’ devilry or defense mechanism of the host?
Author(s) -
Montes Carolina L.,
AcostaRodríguez Eva V.,
Merino Maria Cecilia,
Bermejo Daniela A.,
Gruppi Adriana
Publication year - 2007
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.0407214
Subject(s) - polyclonal antibodies , polyclonal b cell response , biology , antibody , immune system , immunology , b cell , antigen , memory b cell , microbiology and biotechnology , b cell receptor
Polyclonal B cell activation is not a peculiar characteristic to a particular infection, as many viruses, bacteria, and parasites induce a strong polyclonal B cell response resulting in hyper‐γ‐globulinemia. Here, we discuss the different roles proposed for polyclonal B cell activation, which can be crucial for early host defense against rapidly dividing microorganisms by contributing antibodies specific for a spectrum of conserved structures present in the pathogens. In addition, polyclonal B cell activation can be responsible for maintenance of memory B cell responses because of the continuous, unrestricted stimulation of memory B cells whose antibody production may be sustained in the absence of the antigens binding‐specific BCR. Conversely, polyclonal activation can be triggered by microorganisms to avoid the host‐specific, immune response by activating B cell clones, which produce nonmicroorganism‐specific antibodies. Finally, some reports suggest a deleterious role for polyclonal activation, arguing that it could potentially turn on anti‐self‐responses and lead to autoimmune manifestations during chronic infections.