Abstract:
:An immunosuppressed rat model of Pneumocystis carinii pneumonia is described that utilizes simple, noninvasive intratracheal (i.t.) inoculation of cryopreserved parasites and results in development of severe P. carinii pneumonia within 5 weeks. This is an improvement over the most commonly used models of P. carinii pneumonia that rely on immune suppression to activate latent P. carinii infections and that often require 8 to 12 weeks to produce heavy infections of P. carinii. It is also less labor intensive than more recent models requiring surgical instillation of parasites. Our report describes a series of preliminary studies to select an appropriate strain of rat; to determine suitable methods for inducing uniform immunosuppression, P. carinii inoculation, and laboratory maintenance of P. carinii; and to determine effective animal husbandry methods for maintaining animals free from serious secondary infections. Results of our more detailed studies demonstrate that animals receiving two or three i.t. inoculations of approximately 10(6) cryopreserved P. carinii organisms have a predictable course of disease progression which includes moderate P. carinii infections within 3 weeks, severe P. carinii pneumonia in 5 weeks, and a high percentage of mortality due to P. carinii pneumonia in 6 weeks. Parasites were distributed evenly between the right and left lungs, regardless of the number of P. carinii inoculations administered. Non-P. carinii-inoculated immunosuppressed control rats maintained in microisolator cages remained free of P. carinii, thus providing an important control that is missing from many P. carinii pneumonia models. Most non-P. carinii-inoculated control animals and P. carinii-inoculated rats treated with trimethoprim-sulfamethoxazole that were housed in open caging in the same room containing heavily infected animals had no detectable infections after 5 to 6 weeks of immunosuppression; however, some had a small number of P. carinii in their lungs. Because heavy, reproducible infections are achieved 5 weeks after i.t. inoculation, because few animals are lost to secondary infections, and because animals can be maintained as noninfected contemporaneous controls, this animal model is useful for the maintenance of P. carinii strains, for studies of the transmission and natural history of P. carinii, for the production of large numbers of organisms for laboratory studies, and for the evaluation of potential anti-P. carinii drugs.
journal_name
Infect Immunjournal_title
Infection and immunityauthors
Boylan CJ,Current WLdoi
10.1128/IAI.60.4.1589-1597.1992keywords:
subject
Has Abstractpub_date
1992-04-01 00:00:00pages
1589-97issue
4eissn
0019-9567issn
1098-5522journal_volume
60pub_type
杂志文章abstract::Results from studies using mice deficient in specific complement factors and clinical data on patients with an inherited deficiency of the classical complement pathway component C2 suggest that the classical pathway is vital for immunity to Streptococcus pneumoniae. However, the consequences of defects in classical pa...
journal_title:Infection and immunity
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doi:10.1128/IAI.00291-08
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abstract::Peritoneal exudate T lymphocytes from Listeria monocytogenes-immune mice in the presence of the homologous antigen (heat-killed L. monocytogenes) and normal macrophages showed L. monocytogenes-specific proliferative responses. Proliferation was inhibited by macrophages from L. monocytogenes- or Corynebacterium parvum-...
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doi:10.1128/IAI.38.3.907-913.1982
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abstract::The antigenically variant Chlamydia trachomatis major outer membrane protein (MOMP) is a target of antibody-mediated neutralization in vitro, and it is an important protein for designing a subunit vaccine. Knowledge of MOMP T-cell determinants will be essential to elicit rapid and strong immune responses following an ...
journal_title:Infection and immunity
pub_type: 杂志文章
doi:10.1128/IAI.60.9.3714-3718.1992
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abstract::Two distinct monoclonal antibodies, one to pertussis toxin subunit S2, called 9G8, and another to subunits S2 and S3, called 11E6, were generated from the hybridomas of myeloma SP2/0 and spleen cells of BALB/c mice immunized mainly with the subunit S234 complex. Binding ability of 9G8 and 11E6 to the subunits was conf...
journal_title:Infection and immunity
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doi:10.1128/IAI.55.4.909-915.1987
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journal_title:Infection and immunity
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journal_title:Infection and immunity
pub_type: 杂志文章
doi:10.1128/IAI.22.3.908-918.1978
更新日期:1978-12-01 00:00:00
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doi:10.1128/IAI.67.9.4557-4562.1999
更新日期:1999-09-01 00:00:00
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journal_title:Infection and immunity
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更新日期:2009-05-01 00:00:00
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journal_title:Infection and immunity
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doi:10.1128/IAI.52.1.209-212.1986
更新日期:1986-04-01 00:00:00
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doi:10.1128/IAI.50.2.488-494.1985
更新日期:1985-11-01 00:00:00
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pub_type: 杂志文章
doi:10.1128/IAI.01397-13
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journal_title:Infection and immunity
pub_type: 杂志文章
doi:10.1128/IAI.11.4.727-731.1975
更新日期:1975-04-01 00:00:00
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doi:10.1128/IAI.62.6.2195-2201.1994
更新日期:1994-06-01 00:00:00
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journal_title:Infection and immunity
pub_type: 杂志文章
doi:10.1128/IAI.44.2.534-536.1984
更新日期:1984-05-01 00:00:00
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更新日期:1999-12-01 00:00:00
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journal_title:Infection and immunity
pub_type: 杂志文章
doi:10.1128/IAI.66.7.3232-3241.1998
更新日期:1998-07-01 00:00:00
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journal_title:Infection and immunity
pub_type: 杂志文章
doi:10.1128/IAI.4.6.715-719.1971
更新日期:1971-12-01 00:00:00
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journal_title:Infection and immunity
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journal_title:Infection and immunity
pub_type: 杂志文章
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更新日期:1985-05-01 00:00:00
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journal_title:Infection and immunity
pub_type: 杂志文章
doi:10.1128/IAI.56.1.213-218.1988
更新日期:1988-01-01 00:00:00
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journal_title:Infection and immunity
pub_type: 杂志文章
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