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Zinc level and prevalence of rejection in transplanted patients.

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TLDR
Zinc deficiency was accompanied by the qualities and functional insufficiency of T-cell mediated immunity and by diminished phagocytic activity of neutrophils as discussed by the authors, which may cause rejection in the allograft organ.
Abstract
Dear Editor, High zinc level by promoting the immune system may cause rejection in the allograft organ. So it seems that limitation of zinc supplement and all foods and drugs with high amount of zinc may be effective in prevention of rejection after transplantation. Zinc is an essential micronutrient for human growth, development and immune function. Zinc deficiency was accompanied by the qualities and functional insufficiency of T-cell mediated immunity and by the diminished phagocytic activity of neutrophils.[1] Kabu et al. in July 2006 revealed that zinc was involved in multiple step of FC epsilon RI-induced mast cell activation and required for degranulation of cytokines such as IL-6 and TNF-α production and lymphocytes proliferation.[1][2] In study by Chen et al. (Nov 2005) on the effects of different levels of zinc nutrition status on the immune function of mice spleen lymphocytes showed that zinc status affected the immune function and production of IL-2 in spleen lymphocytes [3] Rejection is one of the most important problems after organ transplantation. Immune system has a critical role in this process .In the context of allograft rejection, T cells play a central role in the immune response, once activated, they secrete cytokines and chemokines to activate and attract cells such as CD8 T cells and macrophages into the allograft. They also interact with B cells that secrete alloreactive antibodies that eventually lead to allograft destruction. [4] Moreover transplant rejection has both cellular and humeral components, some of the cytokines produced by T cells and macrophages (TNF-α) may mediate apoptosis of graft cells. [5] According to all those facts, it could be hypothesized that high zinc level by promoting the immune system may cause rejection in the allograft organ.

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Journal ArticleDOI

T-cell allorecognition and transplant rejection: a summary and update.

TL;DR: The findings suggest that the survival and the histologic features of a transplanted organ are influenced not only by the T‐cell recognition pathway, but also by the frequency, the induced effector functions and the specific cellular targets of the alloreactive T‐ cell repertoire.
Journal ArticleDOI

Zinc Is Required for FcεRI-Mediated Mast Cell Activation

TL;DR: It was found that Zn was required for FcεRI-induced translocation of granules to the plasma membrane, a process that has been shown to be important for MC degranulation, and it was showed that a Zn chelator inhibited in vivo allergic reactions such as PCA and PSA.
Journal Article

The alloimmune response and effector mechanisms of allograft rejection.

TL;DR: Novel insights into the interactions between antigen presenting cells and T lymphocytes, and further understanding of how alloimmune responses are regulated, will help in developing effective antirejection and tolerance-inducing strategies.
Journal ArticleDOI

Serum levels of interleukin (IL)-10, IL-17, transforming growth factor (TGF)-β1, and interferon-γ cytokines and expression levels of IL-10 and TGF-β1 genes in renal allograft recipients after donor bone marrow cell infusion.

TL;DR: The decreased levels of inflammatory cytokines besides IL-10 with increased TGF-β1 levels and better allograft function with improved clinical outcomes were observed among infused patients, possibly indicating immunomodulatory effects of this approach in kidney allografted patients.
Journal Article

The Predictive Value of HLA-DR Matching and Cytokine Gene Polymorphisms in Renal Allograft Acute Rejection: a Living-unrelated Donor (LURD) Study.

TL;DR: It is concluded that a more detailed immunogenetic profile is necessary to predict transplant outcome or immunosuppression tailoring and the predictive value of HLA-DR mismatching for acute rejection is not as reliable as in cadaveric transplant.
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