Abstract

Natural killer (NK) cells are part of the cellular immune response. They target mainly cancer and virally infected cells. To a high extent cytotoxic activity of NK cells is regulated inter alia by signals from killer immunoglobulin-like receptors (KIR). The major histocompatibility complex (MHC) class I molecules are important ligands for KIR receptors. Binding of ligands (such as MHC I) to the KIR receptors has the important role in solid organ or hematopoietic cell transplantation. Of note, the understanding of the relationship between KIR and MHC receptors may contribute to the improvement of transplant results. Donor-recipient matching, which also includes the KIR typing, may improve monitoring, individualize the treatment and allow for predicting possible effects after transplantation, such as the graft-versus-leukemia effect (GvL) or viral re-infection. There are also less evident implications of KIR/MHC matching, such as with pregnancy and cancer. In this review, we present the most relevant literature reports on the importance of the KIR/MHC relationship on NK cell activity and hematopoietic stem cell transplantation (HSCT)/solid organ transplantation (SOT) effects, the risk of allograft rejection, protection against post-transplant cytomegalovirus (CMV) infection, pregnancy complications, cancer and adoptive therapy with NK cells.

Highlights

  • IntroductionPublisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations

  • Reports suggest the importance of interactions between killer immunoglobulin-like receptors (KIR) receptors and human leukocyte antigen (HLA) in predicting the risk of allograft rejection, protection against post-transplant CMV infection, graft-versus-host disease (GVHD) and pregnancy complications [2]

  • Presented the “missing self” hypothesis, which stated that Natural killer (NK) cells kill cells with we presented the “missing self” hypothesis, which stated that NK cells kill cells with weak nonoMHC-I

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Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. The most frequently described mechanism is the relationship of KIR receptors and MHC ligands, but it is known that NK education applies to other receptor-ligand interactions, for example CD94/NKG2A and LIR family receptors that bind HLA and increase the potential of NK responses. In light of new reports on NK cell recall/educated responses mediated with cytokines and seen as a kind of immune memory, the role of NK cells on autoreactive and autoinflammatory diseases is extremely interesting [30]. Upon ligand/receptor coupling, depending on the signal, NK cells will be activated or will not react to the target cells This information could be used to predict NK cell responses and possible treatment modifications. KIR genes exist as several allelic forms, which makes them the most poly human family of NK cell receptors.

Methods for KIR Typing
Methods for KIR
10. Therapy
Findings
11. Conclusions
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