Role for T cell-independent B cell activity in the resolution of primary rotavirus infection in mice

Citation
Jl. Vancott et al., Role for T cell-independent B cell activity in the resolution of primary rotavirus infection in mice, EUR J IMMUN, 31(11), 2001, pp. 3380-3387
Citations number
29
Categorie Soggetti
Immunology
Journal title
EUROPEAN JOURNAL OF IMMUNOLOGY
ISSN journal
00142980 → ACNP
Volume
31
Issue
11
Year of publication
2001
Pages
3380 - 3387
Database
ISI
SICI code
0014-2980(200111)31:11<3380:RFTCBC>2.0.ZU;2-R
Abstract
We examined the importance of T cell-independent B cell activity in the res olution of primary murine (EDIM) rotavirus infection in adult mice. We show ed that Rag 1 (C57BL/6 background) and Rag 2 (BALB/c background) knockout m ice, which lack both T and B cells, chronically shed high levels of rotavir us Ag in stool samples following oral inoculation. However, nude mice (BALB /c and C57BL/6 backgrounds) and ap TCR knockout mice (C57BL/6 background) c hronically shed 100-fold lower levels of virus in stool samples. Thus, B ce lls appeared to sharply reduce the level of chronic rotavirus shedding by a T cell-independent mechanism. C57BL/6 mice depleted of CD4(+) cells or bot h CD4(+) and CD8(+) cells were also unable to resolve primary rotavirus inf ection but chronically shed equally low levels of rotavirus Ag in stool sam ples, whereas mice depleted of only CD8(+) cells resolved infection. Simila r results were obtained with a second rotavirus strain (ECw) in which virus was shed chronically in stool samples at low levels in alpha beta TCR knoc kout mice and at high levels in Rag 1 knockout mice. Virus-specific intesti nal IgA was readily detected in mice lacking thymic T cells and alpha beta T cells and in mice depleted of CD4(+) cells but levels were 95% reduced in comparison to immunocompetent control mice. Together, these results show t hat B cells lacking CD4(+) T cell help have the capacity to substantially r educe rotavirus shedding, possibly through the production of T cell-indepen dent IgA to rotavirus, but full resolution requires alpha beta T cells.