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cells, exosomes, allograft, heart, mice, treg, hearts, fig, article, donorderived, inflammation, immune, cell, results, data, google, scholar, transplantation, gata, par, isolated, donor, mmpa, foxp, specific, levels, showed, cas, show, induce, antigen, group, flow, day, frequency, nature, cytometry, treated, analyzed, mouse, regulatory, rejection, exosome, extracts, mononuclear, culture, ova, survival, image, bars,

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nature portfolio cardiovascular translational research privacy policy nature advertising cell-mediated delayed-type hypersensitivity social media 0/ reprints commercial reagent kits donor-derived exosomes inhibits alloreactive delayed-type hypersensitivity enzyme-linked immunosorbent assay donor-derived peripheral exosomes cardiovascular endothelium-derived exosomes donor-derived exosomes induced antigen-specific th2 cells donor-derived exosomes died donor-specific th2 cells real time rt-pcr par2-mediated gata3 suppression donor antigen-specific donor antigen specific donor-derived exosome immunization ova-specific th2 cells permissions author correspondence elisa kits transplantation-induced immune inflammation author correction allograft-induced th2 inflammation th1 cytokine ifn-γ immature dendritic cells induce immune tolerance exosome-conducted inhibitory effect long-term survival donor-derived exosome anti-ifn-γ antibody exosome-induced foxp3 expression donor-derived exosomes donor-derived exosomes giant cell myocarditis th1 pattern-inflammation plays full size image donor tissue tolerance privacy mononuclear cell infiltration inducing allograft tolerance human subjects magnetic cell sorting antibody-protein-dna complex

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         headline:Donor-derived exosomes induce specific regulatory T cells to suppress immune inflammation in the allograft heart
         description:To inhibit the immune inflammation in the allografts can be beneficial to organ transplantation. This study aims to induce the donor antigen specific regulatory T cells (Treg cell) inhibit the immune inflammation in the allograft heart. In this study, peripheral exosomes were purified from the mouse serum. A heart transplantation mouse model was developed. The immune inflammation of the allograft heart was assessed by histology and flow cytometry. The results showed that the donor antigen-specific T helper (Th)2 pattern inflammation was observed in the allograft hearts; the inflammation was inhibited by immunizing the recipient mice with the donor-derived exosomes. Purified peripheral exosomes contained integrin MMP1a; the latter induced CD4+ T cells to express Fork head protein-3 and transforming growth factor (TGF)-β via inhibiting the Th2 transcription factor, GATA binding protein 3, in CD4+ T cells. Administration with the donor-derived exosomes significantly prolonged the allograft heart survival. We conclude that the donor-derived peripheral exosomes have the capacity to inhibit the immune inflammation in the allograft heart via inducing specific Treg cells, implicating that administration with the donor-derived exosomes may be beneficial to cardiac transplantation.
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      headline:Donor-derived exosomes induce specific regulatory T cells to suppress immune inflammation in the allograft heart
      description:To inhibit the immune inflammation in the allografts can be beneficial to organ transplantation. This study aims to induce the donor antigen specific regulatory T cells (Treg cell) inhibit the immune inflammation in the allograft heart. In this study, peripheral exosomes were purified from the mouse serum. A heart transplantation mouse model was developed. The immune inflammation of the allograft heart was assessed by histology and flow cytometry. The results showed that the donor antigen-specific T helper (Th)2 pattern inflammation was observed in the allograft hearts; the inflammation was inhibited by immunizing the recipient mice with the donor-derived exosomes. Purified peripheral exosomes contained integrin MMP1a; the latter induced CD4+ T cells to express Fork head protein-3 and transforming growth factor (TGF)-β via inhibiting the Th2 transcription factor, GATA binding protein 3, in CD4+ T cells. Administration with the donor-derived exosomes significantly prolonged the allograft heart survival. We conclude that the donor-derived peripheral exosomes have the capacity to inhibit the immune inflammation in the allograft heart via inducing specific Treg cells, implicating that administration with the donor-derived exosomes may be beneficial to cardiac transplantation.
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            type:Organization
      name:Kai Chen
      affiliation:
            name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
            address:
               name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
               type:PostalAddress
            type:Organization
      name:Zheng Wang
      affiliation:
            name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
            address:
               name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
               type:PostalAddress
            type:Organization
      name:Pingchang Yang
      affiliation:
            name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
            address:
               name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
               type:PostalAddress
            type:Organization
      name:Shengshou Hu
      affiliation:
            name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
            address:
               name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China
      name:State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Xi Cheng District, China

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