Academic Journal

CD4 + T Cells Are Not Essential for Control of Early Acute Cryptosporidium parvum Infection in Neonatal Mice

التفاصيل البيبلوغرافية
العنوان: CD4 + T Cells Are Not Essential for Control of Early Acute Cryptosporidium parvum Infection in Neonatal Mice
المؤلفون: Korbel, Daniel S., Barakat, Farah M., Di Santo, James P., McDonald, Vincent
المساهمون: Urban, J. F.
المصدر: Infection and Immunity ; volume 79, issue 4, page 1647-1653 ; ISSN 0019-9567 1098-5522
بيانات النشر: American Society for Microbiology
سنة النشر: 2011
الوصف: Cryptosporidiosis is an important diarrheal disease of humans and neonatal livestock caused by Cryptosporidium spp. that infect epithelial cells. Recovery from Cryptosporidium parvum infection in adult hosts involves CD4 + T cells with a strong Th1 component, but mechanisms of immunity in neonates are not well characterized. In the present investigation with newborn mice, similar acute patterns of infection were obtained in C57BL/6 wild-type (WT) and T and B cell-deficient Rag2 −/− mice. In comparison with uninfected controls, the proportion of intestinal CD4 + or CD8 + T cells did not increase in infected WT mice during recovery from infection. Furthermore, infection in neonatal WT mice depleted of CD4 + T cells was not exacerbated. Ten weeks after WT and Rag2 −/− mice had been infected as neonates, no patent infections could be detected. Treatment at this stage with the immunosuppressive drug dexamethasone produced patent infections in Rag2 −/− mice but not WT mice. Expression of inflammatory markers, including gamma interferon (IFN-γ) and interleukin-12p40 (IL-12p40), was higher in neonatal WT mice than in Rag2 −/− mice around the peak of infection, but IL-10 expression was also higher in WT mice. These results suggest that although CD4 + T cells may be important for elimination of C. parvum , these cells are dispensable for controlling the early acute phase of infection in neonates.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1128/iai.00922-10
DOI: 10.1128/IAI.00922-10
الاتاحة: http://dx.doi.org/10.1128/iai.00922-10
https://journals.asm.org/doi/pdf/10.1128/IAI.00922-10
Rights: https://journals.asm.org/non-commercial-tdm-license
رقم الانضمام: edsbas.364A3A35
قاعدة البيانات: BASE