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      KCI등재 SCOPUS SCIE

      Microbial Colonization at Early Life Promotes the Development of Diet-Induced CD8αβ Intraepithelial T Cells

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      https://www.riss.kr/link?id=A106158582

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Intraepithelial lymphocytes (IELs) develop through the continuous interaction with intestinal antigens such as commensal microbiome and diet. However, their respective roles and mutual interactions in the development of IELs are largely unknown. Here, we showed that dietary antigens regulate the development of the majority of CD8αβ IELs in the small intestine and the absence of commensal microbiota particularly during the weaning period, delay the development of IELs. When we tested specific dietary components, such as wheat or combined corn, soybean and yeast, they were dependent on commensal bacteria for the timely development of diet-induced CD8αβ IELs. In addition, supplementation of intestinal antigens later in life was inefficient for the full induction of CD8αβ IELs. Overall, our findings suggest that early exposure to commensal bacteria is important for the proper development of dietary antigen-dependent immune repertoire in the gut.
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      Intraepithelial lymphocytes (IELs) develop through the continuous interaction with intestinal antigens such as commensal microbiome and diet. However, their respective roles and mutual interactions in the development of IELs are largely unknown. Here,...

      Intraepithelial lymphocytes (IELs) develop through the continuous interaction with intestinal antigens such as commensal microbiome and diet. However, their respective roles and mutual interactions in the development of IELs are largely unknown. Here, we showed that dietary antigens regulate the development of the majority of CD8αβ IELs in the small intestine and the absence of commensal microbiota particularly during the weaning period, delay the development of IELs. When we tested specific dietary components, such as wheat or combined corn, soybean and yeast, they were dependent on commensal bacteria for the timely development of diet-induced CD8αβ IELs. In addition, supplementation of intestinal antigens later in life was inefficient for the full induction of CD8αβ IELs. Overall, our findings suggest that early exposure to commensal bacteria is important for the proper development of dietary antigen-dependent immune repertoire in the gut.

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      참고문헌 (Reference)

      1 Chardes, T., "Toxoplasma gondii oral infection induces specific cytotoxic CD8 alpha/beta+ Thy-1+ gut intraepithelial lymphocytes, lytic for parasite-infected enterocytes" 153 : 4596-4603, 1994

      2 Cheroutre, H., "The light and dark sides of intestinal intraepithelial lymphocytes" 11 : 445-456, 2011

      3 Menezes, J. S., "Stimulation by food proteins plays a critical role in the maturation of the immune system" 15 : 447-455, 2003

      4 Hu, M. D., "Sentinels at the frontline : the role of intraepithelial lymphocytes in inflammatory bowel disease" 3 : 321-334, 2017

      5 Bol-Schoenmakers, M., "Regulation by intestinal gammadelta T cells during establishment of food allergic sensitization in mice" 66 : 331-340, 2011

      6 Maynard, C. L., "Reciprocal interactions of the intestinal microbiota and immune system" 489 : 231-241, 2012

      7 Imaoka, A., "Proliferative recruitment of intestinal intraepithelial lymphocytes after microbial colonization of germ-free mice" 26 : 945-948, 1996

      8 Pope, C., "Organ-specific regulation of the CD8 T cell response to Listeria monocytogenes infection" 166 : 3402-3409, 2001

      9 Sheridan, B. S., "Oral infection drives a distinct population of intestinal resident memory CD8(+)T cells with enhanced protective function" 40 : 747-757, 2014

      10 Regnault, A., "Oligoclonal repertoire of the CD8 alpha alpha and the CD8alpha beta TCR-alpha/beta murine intestinal intraepithelial T lymphocytes : evidence for the random emergence of T cells" 180 : 1345-1358, 1994

      1 Chardes, T., "Toxoplasma gondii oral infection induces specific cytotoxic CD8 alpha/beta+ Thy-1+ gut intraepithelial lymphocytes, lytic for parasite-infected enterocytes" 153 : 4596-4603, 1994

      2 Cheroutre, H., "The light and dark sides of intestinal intraepithelial lymphocytes" 11 : 445-456, 2011

      3 Menezes, J. S., "Stimulation by food proteins plays a critical role in the maturation of the immune system" 15 : 447-455, 2003

      4 Hu, M. D., "Sentinels at the frontline : the role of intraepithelial lymphocytes in inflammatory bowel disease" 3 : 321-334, 2017

      5 Bol-Schoenmakers, M., "Regulation by intestinal gammadelta T cells during establishment of food allergic sensitization in mice" 66 : 331-340, 2011

      6 Maynard, C. L., "Reciprocal interactions of the intestinal microbiota and immune system" 489 : 231-241, 2012

      7 Imaoka, A., "Proliferative recruitment of intestinal intraepithelial lymphocytes after microbial colonization of germ-free mice" 26 : 945-948, 1996

      8 Pope, C., "Organ-specific regulation of the CD8 T cell response to Listeria monocytogenes infection" 166 : 3402-3409, 2001

      9 Sheridan, B. S., "Oral infection drives a distinct population of intestinal resident memory CD8(+)T cells with enhanced protective function" 40 : 747-757, 2014

      10 Regnault, A., "Oligoclonal repertoire of the CD8 alpha alpha and the CD8alpha beta TCR-alpha/beta murine intestinal intraepithelial T lymphocytes : evidence for the random emergence of T cells" 180 : 1345-1358, 1994

      11 Helgeland, L., "Microbial colonization induces oligoclonal expansions of intraepithelial CD8 T cells in the gut" 34 : 3389-3400, 2004

      12 Cervantes-Barragan, L., "Lactobacillus reuteri induces gut intraepithelial CD4+CD8αα+ T cells" 357 : 806-810, 2017

      13 Eggesbo, M., "Is delivery by cesarean section a risk factor for food allergy? J" 112 : 420-426, 2003

      14 Anderson, K. G., "Intravascular staining for discrimination of vascular and tissue leukocytes" 9 : 209-222, 2014

      15 Buzoni-Gatel, D., "Intraepithelial lymphocytes traffic to the intestine and enhance resistance to Toxoplasma gondii oral infection" 162 : 5846-5852, 1999

      16 Abadie, V., "Intraepithelial lymphocytes in celiac disease immunopathology" 34 : 551-566, 2012

      17 Sheridan, B. S., "Intraepithelial lymphocytes : to serve and protect" 12 : 513-521, 2010

      18 Kunisawa, J., "Intraepithelial lymphocytes : their shared and divergent immunological behaviors in the small and large intestine" 215 : 136-153, 2007

      19 Williams, A. M., "Intestinal alpha beta T cells differentiate and rearrange antigen receptor genes in situ in the human infant" 173 : 7190-7199, 2004

      20 Cebra, J. J., "Influences of microbiota on intestinal immune system development" 69 : 1046S-1051S, 1999

      21 Ivanov, II, Atarashi, K., "Induction of intestinal Th17 cells by segmented filamentous bacteria" 139 : 485-498, 2009

      22 Tajima, M., "IL-6-dependent spontaneous proliferation is required for the induction of colitogenic IL-17-producing CD8+ T cells" 205 : 1019-1027, 2008

      23 Latthe, M., "High frequency of CD8 alpha alpha homodimer-bearing T cells in human fetal intestine" 24 : 1703-1705, 1994

      24 Lepage, A. C., "Gut-derived intraepithelial lymphocytes induce long term immunity against Toxoplasma gondii" 161 : 4902-4908, 1998

      25 Chung, H., "Gut immune maturation depends on colonization with a host-specific microbiota" 149 : 1578-1593, 2012

      26 Catalan-Serra, I., "Gammadelta T cells in crohn's disease: a new player in the disease pathogenesis?" 11 : 1135-1145, 2017

      27 Regner, E. H., "Functional intraepithelial lymphocyte changes in inflammatory bowel disease and spondyloarthritis have disease specific correlations with intestinal microbiota" 20 : 149-, 2018

      28 Umesaki, Y., "Expansion of alpha beta T-cell receptor-bearing intestinal intraepithelial lymphocytes after microbial colonization in germ-free mice and its independence from thymus" 79 : 32-37, 1993

      29 Mercer, N., "Duodenal intraepithelial lymphocytes of children with cow milk allergy preferentially bind the glycan-binding protein galectin-3" 22 : 207-217, 2009

      30 McDonald, B. D., "Diverse developmental pathways of intestinal intraepithelial lymphocytes" 18 : 514-525, 2018

      31 Umesaki, Y., "Differential roles of segmented filamentous bacteria and clostridia in development of the intestinal immune system" 67 : 3504-3511, 1999

      32 Kim, K. S., "Dietary antigens limit mucosal immunity by inducing regulatory T cells in the small intestine" 351 : 858-863, 2016

      33 Kawaguchi-Miyashita, M., "Development and cytolytic function of intestinal intraepithelial T lymphocytes in antigen-minimized mice" 89 : 268-273, 1996

      34 Anderson, K. G., "Cutting edge : intravascular staining redefines lung CD8 T cell responses" 189 : 2702-2706, 2012

      35 이경희, "Cigarette Smoke Extract Enhances IL-17A-Induced IL-8 Production via Up-Regulation of IL-17R in Human Bronchial Epithelial Cells" 한국분자세포생물학회 41 (41): 282-289, 2018

      36 Eggesbo, M., "Cesarean delivery and cow milk allergy/intolerance" 60 : 1172-1173, 2005

      37 Pleasants, J. R., "Adequacy of chemically defined, water-soluble diet for germfree BALB/c mice through successive generations and litters" 116 : 1949-1964, 1986

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      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
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      2008-01-01 평가 SCI 등재 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1998-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 2.77 0.19 1.85
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.37 1.11 0.379 0.03
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