Interrelation Between Fibroblasts and T Cells in Fibrosing Interstitial Lung Diseases

被引:19
作者
Lai, Yunxin [1 ]
Wei, Xinru [1 ]
Ye, Ting [1 ]
Hang, Lilin [2 ]
Mou, Ling [1 ]
Su, Jin [1 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 1, Guangzhou Inst Resp Hlth, State Key Lab Resp Dis,Natl Clin Res Ctr Resp Dis, Guangzhou, Guangdong, Peoples R China
[2] Southern Med Univ, Zhujiang Hosp, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
fibroblasts; T cells; interrelation; ILDs; fibrosis; HUMAN DERMAL FIBROBLASTS; FAS-MEDIATED APOPTOSIS; COLLAGEN PRODUCTION; PULMONARY-FIBROSIS; SYSTEMIC-SCLEROSIS; RESIDENT FIBROBLASTS; TH17; CELLS; EXPRESSION; PROLIFERATION; INFLAMMATION;
D O I
10.3389/fimmu.2021.747335
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interstitial lung diseases (ILDs) are a heterogeneous group of diseases characterized by varying degrees of inflammation and fibrosis of the pulmonary interstitium. The interrelations between multiple immune cells and stromal cells participate in the pathogenesis of ILDs. While fibroblasts contribute to the development of ILDs through secreting extracellular matrix and proinflammatory cytokines upon activation, T cells are major mediators of adaptive immunity, as well as inflammation and autoimmune tissue destruction in the lung of ILDs patients. Fibroblasts play important roles in modulating T cell recruitment, differentiation and function and conversely, T cells can balance fibrotic sequelae with protective immunity in the lung. A more precise understanding of the interrelation between fibroblasts and T cells will enable a better future therapeutic design by targeting this interrelationship. Here we highlight recent work on the interactions between fibroblasts and T cells in ILDs, and consider the implications of these interactions in the future development of therapies for ILDs.
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页数:12
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共 130 条
[1]  
Adami E., 2021, RHEUMATOL OXFORD, DOI [10.1093/rheumatology/keab168, DOI 10.1093/RHEUMATOLOGY/KEAB168]
[2]   Blockade of PD-1/PD-L1 Pathway Enhances the Antigen-Presenting Capacity of Fibrocytes [J].
Afroj, Tania ;
Mitsuhashi, Atsushi ;
Ogino, Hirokazu ;
Saijo, Atsuro ;
Otsuka, Kenji ;
Yoneda, Hiroto ;
Tobiume, Makoto ;
Na Thi Nguyen ;
Goto, Hisatsugu ;
Koyama, Kazuya ;
Sugimoto, Masamichi ;
Kondoh, Osamu ;
Nokihara, Hiroshi ;
Nishioka, Yasuhiko .
JOURNAL OF IMMUNOLOGY, 2021, 206 (06) :1204-1214
[3]   Targeting cardiac fibrosis with engineered T cells [J].
Aghajanian, Haig ;
Kimura, Toru ;
Rurik, Joel G. ;
Hancock, Aidan S. ;
Leibowitz, Michael S. ;
Li, Li ;
Scholler, John ;
Monslow, James ;
Lo, Albert ;
Han, Wei ;
Wang, Tao ;
Bedi, Kenneth ;
Morley, Michael P. ;
Saldana, Ricardo A. Linares ;
Bolar, Nikhita A. ;
McDaid, Kendra ;
Assenmacher, Charles-Antoine ;
Smith, Cheryl L. ;
Wirth, Dagmar ;
June, Carl H. ;
Margulies, Kenneth B. ;
Jain, Rajan ;
Pure, Ellen ;
Albelda, Steven M. ;
Epstein, Jonathan A. .
NATURE, 2019, 573 (7774) :430-+
[4]   Matrix metalloproteinases cleave membrane-bound PD-L1 on CD90+ (myo-)fibroblasts in Crohn's disease and regulate Th1/Th17 cell responses [J].
Aguirre, Jose E. ;
Beswick, Ellen J. ;
Grim, Carl ;
Uribe, Gabriela ;
Tafoya, Marissa ;
Palma, Gabriela Chacon ;
Samedi, Von ;
McKee, Rohini ;
Villeger, Romain ;
Fofanov, Yuriy ;
Cong, Yingzi ;
Yochum, Gregory ;
Koltun, Walter ;
Powell, Don ;
Pinchuk, Irina, V .
INTERNATIONAL IMMUNOLOGY, 2020, 32 (01) :57-68
[6]  
Atabati Elham, 2020, Can J Respir Ther, V56, P1, DOI 10.29390/cjrt-2020-021
[7]   Cellular interactions in the pathogenesis of interstitial lung diseases [J].
Bagnato, Gianluca ;
Harari, Sergio .
EUROPEAN RESPIRATORY REVIEW, 2015, 24 (135) :102-114
[8]   Fibrocytes are potent stimulators of anti-virus cytotoxic T cells [J].
Balmelli, C ;
Ruggli, N ;
McCullough, K ;
Summerfield, A .
JOURNAL OF LEUKOCYTE BIOLOGY, 2005, 77 (06) :923-933
[9]   The impact of oxidative DNA damage and stress on telomere homeostasis [J].
Barnes, Ryan P. ;
Fouquerel, Elise ;
Opresko, Patricia L. .
MECHANISMS OF AGEING AND DEVELOPMENT, 2019, 177 :37-45
[10]   Stromal Fibroblasts in Tertiary Lymphoid Structures: A Novel Target in Chronic inflammation [J].
Barone, Francesca ;
Gardner, David H. ;
Nayar, Saba ;
Steinthal, Nathalie ;
Buckley, Christopher D. ;
Luther, Sanjiv A. .
FRONTIERS IN IMMUNOLOGY, 2016, 7