BALB/c and C57BL/6 mice were infected with murine cytomegalovirus (MCMV). On day 4 or 12 of the infection, the animals were immunized with SRBC (T-dependent), TNP-Ficoll (T-independent) and standard poliovirus. The adverse effect of the virus infection on humoral immune responses was limited to animals immunized on day 4; while anti-SRBC antibody formation was severely depressed in both mouse strains, reduced plaque forming cells to TNP-Ficoll were registered only in BALB/c mice. Antibodies to poliovirus were depressed in both strains, although to a lesser degree in C57Bl/6 than in BALB/c mice. Anti-SRBC B cell memory was found to be affected by MCMV infection. These results are interpreted to mean that T-dependent and -independent antigens may be handled differently by the two mouse strains tested.
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http://dx.doi.org/10.1016/S0171-2985(87)80080-3 | DOI Listing |
Pathogens
December 2024
Center for Proteomics, Faculty of Medicine, University of Rijeka, 51000 Rijeka, Croatia.
Human cytomegalovirus (HCMV) rarely infects the brain following infection of adult individuals. However, the virus readily infects the brain during congenital HCMV (cHCMV) infection, frequently causing severe neurodevelopmental and neurological sequelae. Interestingly, although the incidence of cHCMV infection is 0.
View Article and Find Full Text PDFCell Rep Med
January 2025
Vyriad Inc, Rochester, MN 55901, USA. Electronic address:
Cytomegalovirus (CMV) infects a wide range of cell types, including tumor-associated myeloid cells and glioma cells. Clinical observations suggest a potential link between long-term glioblastoma survival and CMV reactivation. We herein present an oncolytic CMV vector, AD169r, which includes a restored pentamer complex gH/gL/pUL128-131 and the removal of UL1-UL20 and UL/b' sequences.
View Article and Find Full Text PDFJ Exp Med
March 2025
Institute of Experimental Immunology, University of Zürich, Zürich, Switzerland.
Group 1 innate lymphoid cells (ILCs) encompass NK cells and ILC1s, which have non-redundant roles in host protection against pathogens and cancer. Despite their circulating nature, NK cells can establish residency in selected tissues during ontogeny, forming a distinct functional subset. The mechanisms that initiate, maintain, and regulate the conversion of NK cells into tissue-resident NK (trNK) cells are currently not well understood.
View Article and Find Full Text PDFSci Adv
November 2024
Department of Microbiology and Immunology, Jefferson Center for Vaccines and Pandemic Preparedness, Sidney Kimmel Medical College, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Human cytomegalovirus (CMV) causes a common congenital infection leading to long-term neurological impairments including brain, cochlear, and ocular pathology. Infection of newborn mice with murine (M)CMV is an established model of neuropathology caused by congenital CMV infection, with recent work suggesting that brain pathology may be driven by immune responses. In the eye, however, CMV retinitis is thought to result from virus-driven necrosis in the absence of T cell responses.
View Article and Find Full Text PDFUnlabelled: Cytomegaloviruses are highly species-specific as they replicate only in cells of their own or a closely related species. For instance, human cytomegalovirus cannot replicate in rodent cells, and mouse cytomegalovirus (MCMV) cannot replicate in human and monkey cells. However, the mechanisms underlying the host species restriction remain poorly understood.
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