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Untitled - D Ank Unlimited

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B lymphocyte stimulator (BlyS) 97 Bacillus anthracis immunity<br />

B cells<br />

B cells<br />

Antigen<br />

Spleen<br />

No Growth Growth<br />

B Lymphocyte receptor<br />

PEG<br />

To<br />

HAT medium<br />

Hybridoma<br />

B lymphocyte hybridoma.<br />

B lymphocyte receptor.<br />

HGPRT - Myeloma cells<br />

Myeloma<br />

No Growth<br />

are to be distinguished from those in the surrounding<br />

medium that adhere to the B cell surface through Fc receptors.<br />

Refer to membrane immunoglobulin.<br />

B lymphocyte stimulator (BlyS)<br />

A naturally occurring protein that stimulates the immune<br />

system to produce antibodies. It is being tested as a potential<br />

drug for the treatment of immunodeficiency that occurs<br />

in higher than normal levels in rheumatoid arthritis and<br />

lupus patients and could account for their immune systems<br />

becoming overactive and attacking joints in rheumatoid<br />

arthritis (RA) or connective tissues in systemic lupus erythematosus<br />

(SLE).<br />

B lymphocyte stimulatory factors<br />

See interleukins 4, 5, and 6.<br />

B lymphocyte tolerance<br />

Immunologic nonreactivity of B lymphocytes induced by<br />

relatively large doses of antigen. It is of relatively short<br />

duration. By contrast, T cell tolerance requires less antigen<br />

and has a longer duration. Exclusive B cell tolerance leaves<br />

T cells immunoreactive and unaffected.<br />

B-type virus (Aspergillus macaques)<br />

An Old World monkey virus that resembles herpes simplex.<br />

Clinical features include intermittent shedding and reactivation<br />

in the presence of stress and immunosuppression.<br />

Humans who tend these monkeys may become infected<br />

with fatal consequences. B-type viruses possess eccentric<br />

nuclear cores.<br />

babesiosis immunity<br />

The host immune response to babesiosis, a malaria-like disease<br />

transmitted by parasitized Ixodes ticks, depends in part<br />

on the spleen, which has a central role in immune defense.<br />

Patients in whom the spleen has been removed are more<br />

susceptible to infection by Babesia and manifest elevated<br />

parasitemia. Complement activation by Babesia may lead<br />

to formation of TNF-α and IL-1, promoting local defense.<br />

Complement levels decrease in babesiosis. Patients develop<br />

increased circulating C1q binding activity and decreased<br />

C4, C3, and CH50 levels. The formation of TNF-α and IL-1<br />

may account for many of the clinical features of the disease.<br />

Besides macrophages, other cellular immune functions are<br />

critical parts of the response to Babesia. T cell-deficient<br />

mice manifest significantly increased parasitemia. Cellular<br />

immunity is diminished by the disease, which is also<br />

associated with increased CD8 + T lymphocytes, diminished<br />

monocyte mitogen responsiveness, and polyclonal<br />

hypergammaglobulinemia.<br />

bacille Calmette-Guérin<br />

An attenuated strain of Mycobacterium bovis that has<br />

been employed as a vaccine against tuberculosis. Refer to<br />

BCG.<br />

Bacillus anthracis immunity<br />

Protective immunity against anthrax is induced only by<br />

the antigen designated PA. The B. anthracis polypeptide<br />

capsule is only weakly immunogenic and is not believed to<br />

contribute to naturally acquired immunity or induce protection<br />

against anthrax. The Ca – /tx + strains of B. anthracis<br />

are protective. One of these strains is used to prepare a<br />

very successful live-spore animal vaccine. It is considered<br />

unsuitable in the West for use in humans because it retains<br />

some residual virulence. Human vaccine developed half<br />

a century ago consists of aluminum hydroxide-adsorbed,<br />

cell-free filtrates of cultures of a noncapsulating, nonproteolytic<br />

derivative of strain V770. Several doses are<br />

required. An immune response to PA but not to LF or<br />

EF is critical for protection. Immunization with strains<br />

synthesizing either PA and EF or PA and LF resulted in<br />

higher antibody responses to EF or LF, respectively. There<br />

is a synergistic relationship between PA and LF or EF in<br />

immunoprotection. Some cellular immune mechanisms<br />

are believed to be significant in the induction of protective<br />

immunity. PA has been shown with monoclonal antibodies<br />

to have at least three non-overlapping antigenic regions.<br />

It is anticipated that the elucidation of protective motifs<br />

on PA may lead to the development of a subunit-based<br />

vaccine. Passive immunity in the treatment of anthrax has<br />

been unsuccessful.<br />

B

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