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자료유형
학술저널
저자정보
Hye-Ju Han (Kangwon National University) Young-Saeng Jang (Kangwon National University) Goo-Young Seo (Kangwon National University) Sung-Gyoo Park (Gwangju Institute of Science and Technology) Seung Goo Kang (Kangwon National University) Sung-il Yoon (Kangwon National University) Hyun-Jeong Ko (Kangwon National University) Geun-Shik Lee (Kangwon National University) Pyeung-Hyeun Kim (Kangwon National University)
저널정보
대한면역학회 Immune Network Immune Network Vol.18 No.4
발행연도
2018.8
수록면
55 - 67 (13page)

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γδ T cells are abundant in the gut mucosa and play an important role in adaptive immunity as well as innate immunity. Although γδ T cells are supposed to be associated with the enhancement of Ab production, the status of γδ T cells, particularly in the synthesis of IgA isotype, remains unclear. We compared Ig expression in T cell receptor delta chain deficient (TCRδ<SUP>+</SUP>) mice with wild-type mice. The amount of IgA in fecal pellets was substantially elevated in TCRδ<SUP>+</SUP> mice. This was paralleled by an increase in surface IgA expression and total IgA production by Peyer"s patches (PPs) and mesenteric lymph node (MLN) cells. Likewise, the TCRδ<SUP>+</SUP> mice produced much higher levels of serum IgA isotype. Here, surface IgA expression and number of IgA secreting cells were also elevated in the culture of spleen and bone marrow (BM) B cells. Germ-line α transcript, an indicator of IgA class switch recombination, higher in PP and MLN B cells from TCRδ<SUP>+</SUP> mice, while it was not seen in inactivated B cells. Nevertheless, the frequency of IgA<SUP>+</SUP> B cells was much higher in the spleen from TCRδ<SUP>+</SUP> mice. These results suggest that γδ T cells control the early phase of B cells, in order to prevent unnecessary IgA isotype switching. Furthermore, this regulatory role of γδ T cells had lasting effects on the long-lived IgA-producing plasma cells in the BM.

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ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2018-517-003392100