Pneumocystis carinii Infection in Transgenic B Cell-Deficient Mice

Pneumocystis carinii is an important cause of pneumonia in immunocompromised hosts. Both cellular and humoral immunity seem important in resistance to this pathogen, but the specific role of each component is poorly understood. An outbreak of P. carinii pneumonia in transgenic B cell-deficient mice...

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Veröffentlicht in:The Journal of infectious diseases 1996-04, Vol.173 (4), p.1034-1037
Hauptverfasser: Marcotte, Harold, Lévesque, Denise, Delanay, Kathleen, Bourgeault, Andrée, de la Durantaye, Roger, Brochu, Steve, Lavoie, Marc C.
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container_end_page 1037
container_issue 4
container_start_page 1034
container_title The Journal of infectious diseases
container_volume 173
creator Marcotte, Harold
Lévesque, Denise
Delanay, Kathleen
Bourgeault, Andrée
de la Durantaye, Roger
Brochu, Steve
Lavoie, Marc C.
description Pneumocystis carinii is an important cause of pneumonia in immunocompromised hosts. Both cellular and humoral immunity seem important in resistance to this pathogen, but the specific role of each component is poorly understood. An outbreak of P. carinii pneumonia in transgenic B cell-deficient mice (µMT) was studied. Over 4 months, >50% of 41 µMT/µMT mice maintained in a sterile environment died of pneumonia. Some mice had concurrent infection with Pasteurella pneumotropica. Homozygous µMT/µMT mice had no detectable serum immunoglobulins, while their heterozygous µMT/+ counterparts had normal levels of IgM, IgG, and IgA and did not develop pneumonia. The infection was controlled by treating the mice with trimethoprim-sulfamethoxazole, and the pathogen was eliminated by cesarean rederivation. These observations suggest an important role for B cells in the host defense against P. carinii.
doi_str_mv 10.1093/infdis/173.4.1034
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Both cellular and humoral immunity seem important in resistance to this pathogen, but the specific role of each component is poorly understood. An outbreak of P. carinii pneumonia in transgenic B cell-deficient mice (µMT) was studied. Over 4 months, &gt;50% of 41 µMT/µMT mice maintained in a sterile environment died of pneumonia. Some mice had concurrent infection with Pasteurella pneumotropica. Homozygous µMT/µMT mice had no detectable serum immunoglobulins, while their heterozygous µMT/+ counterparts had normal levels of IgM, IgG, and IgA and did not develop pneumonia. The infection was controlled by treating the mice with trimethoprim-sulfamethoxazole, and the pathogen was eliminated by cesarean rederivation. 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Both cellular and humoral immunity seem important in resistance to this pathogen, but the specific role of each component is poorly understood. An outbreak of P. carinii pneumonia in transgenic B cell-deficient mice (µMT) was studied. Over 4 months, &gt;50% of 41 µMT/µMT mice maintained in a sterile environment died of pneumonia. Some mice had concurrent infection with Pasteurella pneumotropica. Homozygous µMT/µMT mice had no detectable serum immunoglobulins, while their heterozygous µMT/+ counterparts had normal levels of IgM, IgG, and IgA and did not develop pneumonia. The infection was controlled by treating the mice with trimethoprim-sulfamethoxazole, and the pathogen was eliminated by cesarean rederivation. These observations suggest an important role for B cells in the host defense against P. carinii.</description><subject>Amibiasis</subject><subject>Animals</subject><subject>Animals, Laboratory - microbiology</subject><subject>B lymphocytes</subject><subject>B-Lymphocytes - immunology</subject><subject>Biological and medical sciences</subject><subject>Concise Communications</subject><subject>Dysgammaglobulinemia - genetics</subject><subject>Dysgammaglobulinemia - immunology</subject><subject>Dysgammaglobulinemia - microbiology</subject><subject>Genes, Immunoglobulin</subject><subject>Human mycoses</subject><subject>Human protozoal diseases</subject><subject>Immunoglobulin mu-Chains - genetics</subject><subject>Immunoglobulins</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Lung - microbiology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Miscellaneous</subject><subject>Mycoses</subject><subject>Mycoses of the respiratory system</subject><subject>Parasitic diseases</subject><subject>Pathogens</subject><subject>Pneumocystis - immunology</subject><subject>Pneumocystis carinii</subject><subject>Pneumocystis pneumonia</subject><subject>Pneumonia</subject><subject>Pneumonia, Pneumocystis - immunology</subject><subject>Pneumonia, Pneumocystis - veterinary</subject><subject>Protozoal diseases</subject><subject>Pulmonary alveoli</subject><subject>T lymphocytes</subject><subject>Viruses</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PGzEQhq2qFQ20P4BDpT1U3BZm_Ll7LKF8SKTtgUpRL5Z34kWmiRfsjVT-PY4SPm49jeT3nUfjh7FDhGOEVpyE2C9CPkEjjmV5EfIdm6ASptYaxXs2AeC8xqZtP7L9nO8AQApt9theo0G00kzY6a_o16uBHvMYckUuhRhCdRV7T2MYYhVidZNczLc-BqpOq6lfLusz3wcKPo7VLJD_xD70bpn95908YL_Pv99ML-vrnxdX02_XNSmuxlpKxbGRHhwH8o0jAVqC6NQCgTpSre44IRrea6OcanpySgpA33WdB92JA3a05d6n4WHt82hXIVO5x0U_rLM1Tfmels1_i6g0GNXyUsRtkdKQc_K9vU9h5dKjRbAbwXYr2BbBVtqN4LLzZQdfdyu_eNnYGS35113uMrllX-RRITzXRGHoVr1i7vI4pDcxCq5xg6m3ecij__eSu_TXaiOMspfzPxYvcDab_5hbJZ4AEYicGg</recordid><startdate>19960401</startdate><enddate>19960401</enddate><creator>Marcotte, Harold</creator><creator>Lévesque, Denise</creator><creator>Delanay, Kathleen</creator><creator>Bourgeault, Andrée</creator><creator>de la Durantaye, Roger</creator><creator>Brochu, Steve</creator><creator>Lavoie, Marc C.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>19960401</creationdate><title>Pneumocystis carinii Infection in Transgenic B Cell-Deficient Mice</title><author>Marcotte, Harold ; 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subjects Amibiasis
Animals
Animals, Laboratory - microbiology
B lymphocytes
B-Lymphocytes - immunology
Biological and medical sciences
Concise Communications
Dysgammaglobulinemia - genetics
Dysgammaglobulinemia - immunology
Dysgammaglobulinemia - microbiology
Genes, Immunoglobulin
Human mycoses
Human protozoal diseases
Immunoglobulin mu-Chains - genetics
Immunoglobulins
Infections
Infectious diseases
Lung - microbiology
Medical sciences
Mice
Mice, Knockout
Miscellaneous
Mycoses
Mycoses of the respiratory system
Parasitic diseases
Pathogens
Pneumocystis - immunology
Pneumocystis carinii
Pneumocystis pneumonia
Pneumonia
Pneumonia, Pneumocystis - immunology
Pneumonia, Pneumocystis - veterinary
Protozoal diseases
Pulmonary alveoli
T lymphocytes
Viruses
title Pneumocystis carinii Infection in Transgenic B Cell-Deficient Mice
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