Matches in SemOpenAlex for { <https://semopenalex.org/work/W2894047470> ?p ?o ?g. }
- W2894047470 endingPage "203" @default.
- W2894047470 startingPage "193" @default.
- W2894047470 abstract "Acute graft-versus-host disease (aGVHD) is an immune-mediated reaction that can occur after hematopoietic stem cell transplantation in which donor T cells recognize the host antigens as foreign, destroying host tissues. Establishment of a tolerogenic immune environment while preserving the immune response to infectious agents is required for successful bone marrow transplantation. Pregnancy-specific glycoprotein 1 (PSG1), which is secreted by the human placenta into the maternal circulation throughout pregnancy, likely plays a role in maintaining immunotolerance to prevent rejection of the fetus by the maternal immune system. We have previously shown that PSG1 activates the latent form of transforming growth factor β1 (TGF-β), a cytokine essential for the differentiation of tolerance-inducing CD4+FoxP3+ regulatory T cells (Tregs). Consistent with this observation, treatment of naïve murine T cells with PSG1 resulted in a significant increase in FoxP3+ cells that was blocked by a TGF-β receptor I inhibitor. We also show here that PSG1 can increase the availability of active TGF-β in vivo. As the role of CD4+FoxP3+ cells in the prevention of aGVHD is well established, we tested whether PSG1 has beneficial effects in a murine aGHVD transplantation model. PSG1-treated mice had reduced numbers of tissue-infiltrating inflammatory CD3+ T cells and had increased expression of FoxP3 in T cells compared with vehicle-treated mice. In addition, administration of PSG1 significantly inhibited aGVHD-associated weight loss and mortality. On the other hand, administration of PSG1 was less effective in managing aGVHD in the presence of an alloimmune reaction against a malignancy in a graft-versus-leukemia experimental model. Combined, this data strongly suggests that PSG1 could be a promising treatment option for patients with aGVHD following bone marrow transplantation for a nonmalignant condition, such as an autoimmune disorder or a genetic immunodeficiency." @default.
- W2894047470 created "2018-10-05" @default.
- W2894047470 creator A5002789970 @default.
- W2894047470 creator A5002882740 @default.
- W2894047470 creator A5013149726 @default.
- W2894047470 creator A5015392494 @default.
- W2894047470 creator A5020046699 @default.
- W2894047470 creator A5040131937 @default.
- W2894047470 creator A5045077371 @default.
- W2894047470 creator A5071756884 @default.
- W2894047470 creator A5090278937 @default.
- W2894047470 date "2019-02-01" @default.
- W2894047470 modified "2023-10-15" @default.
- W2894047470 title "Recombinant Pregnancy-Specific Glycoprotein 1 Has a Protective Role in a Murine Model of Acute Graft-versus-Host Disease" @default.
- W2894047470 cites W1532322008 @default.
- W2894047470 cites W1555220225 @default.
- W2894047470 cites W1556193995 @default.
- W2894047470 cites W1855045052 @default.
- W2894047470 cites W1965052809 @default.
- W2894047470 cites W1976063914 @default.
- W2894047470 cites W1978660935 @default.
- W2894047470 cites W1982325304 @default.
- W2894047470 cites W1987891242 @default.
- W2894047470 cites W1992473112 @default.
- W2894047470 cites W2018919532 @default.
- W2894047470 cites W2019468214 @default.
- W2894047470 cites W2023449596 @default.
- W2894047470 cites W2025833093 @default.
- W2894047470 cites W2027423901 @default.
- W2894047470 cites W2041297370 @default.
- W2894047470 cites W2041827740 @default.
- W2894047470 cites W2045254759 @default.
- W2894047470 cites W2047080123 @default.
- W2894047470 cites W2049783422 @default.
- W2894047470 cites W2053226799 @default.
- W2894047470 cites W2063377993 @default.
- W2894047470 cites W2064957876 @default.
- W2894047470 cites W2066663558 @default.
- W2894047470 cites W2072301202 @default.
- W2894047470 cites W2072632585 @default.
- W2894047470 cites W2077564566 @default.
- W2894047470 cites W2078420687 @default.
- W2894047470 cites W2090043394 @default.
- W2894047470 cites W2113360436 @default.
- W2894047470 cites W2117697495 @default.
- W2894047470 cites W2123368042 @default.
- W2894047470 cites W2123994583 @default.
- W2894047470 cites W2129681072 @default.
- W2894047470 cites W2136180824 @default.
- W2894047470 cites W2143258371 @default.
- W2894047470 cites W2144276864 @default.
- W2894047470 cites W2147068163 @default.
- W2894047470 cites W2149444208 @default.
- W2894047470 cites W2153060237 @default.
- W2894047470 cites W2154568166 @default.
- W2894047470 cites W2157207206 @default.
- W2894047470 cites W2163479283 @default.
- W2894047470 cites W2290901653 @default.
- W2894047470 cites W2305458040 @default.
- W2894047470 cites W2319459971 @default.
- W2894047470 cites W2337723930 @default.
- W2894047470 cites W2398298261 @default.
- W2894047470 cites W2466760217 @default.
- W2894047470 cites W2514964903 @default.
- W2894047470 cites W2574998181 @default.
- W2894047470 cites W2742237928 @default.
- W2894047470 cites W2769222378 @default.
- W2894047470 cites W2793744651 @default.
- W2894047470 cites W4296296481 @default.
- W2894047470 cites W1665070267 @default.
- W2894047470 doi "https://doi.org/10.1016/j.bbmt.2018.09.022" @default.
- W2894047470 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30253241" @default.
- W2894047470 hasPublicationYear "2019" @default.
- W2894047470 type Work @default.
- W2894047470 sameAs 2894047470 @default.
- W2894047470 citedByCount "9" @default.
- W2894047470 countsByYear W28940474702021 @default.
- W2894047470 countsByYear W28940474702022 @default.
- W2894047470 countsByYear W28940474702023 @default.
- W2894047470 crossrefType "journal-article" @default.
- W2894047470 hasAuthorship W2894047470A5002789970 @default.
- W2894047470 hasAuthorship W2894047470A5002882740 @default.
- W2894047470 hasAuthorship W2894047470A5013149726 @default.
- W2894047470 hasAuthorship W2894047470A5015392494 @default.
- W2894047470 hasAuthorship W2894047470A5020046699 @default.
- W2894047470 hasAuthorship W2894047470A5040131937 @default.
- W2894047470 hasAuthorship W2894047470A5045077371 @default.
- W2894047470 hasAuthorship W2894047470A5071756884 @default.
- W2894047470 hasAuthorship W2894047470A5090278937 @default.
- W2894047470 hasBestOaLocation W28940474701 @default.
- W2894047470 hasConcept C109159458 @default.
- W2894047470 hasConcept C126322002 @default.
- W2894047470 hasConcept C203014093 @default.
- W2894047470 hasConcept C2776090121 @default.
- W2894047470 hasConcept C2777702733 @default.
- W2894047470 hasConcept C2778690821 @default.
- W2894047470 hasConcept C2779727006 @default.
- W2894047470 hasConcept C2779972918 @default.