What do hla genes code for




















Bjorkman PJ, Parham P. Structure, function and diversity of class I major histocompatibility complex molecules. Annu Rev Biochem. The structure of HLA-B27 reveals nonamer self-peptides bound in an extended conformation. Klein J, Sato A. The HLA system. First of two parts. N Engl J Med. Engelhard VH. Annu Rev Immunol. Allele-specific motifs revealed by sequencing of self-peptides eluted from MHC molecules. Restriction of in vitro T cell-mediated cytotoxicity in lymphocytic choriomeningitis within a syngeneic or semiallogeneic system.

Specificity pockets for the side chains of peptide antigens in HLA-Aw Antigenic peptide binding by class I and class II histocompatibility proteins. Pamer E, Cresswell P. Mechanisms of MHC class I-restricted antigen processing. Cresswell P. Molecular interactions mediating T cell antigen recognition. Parham P. Immunogenetics of killer-cell immunoglobulin-like receptors.

Microdroplet assay of human serum cytotoxins. Allelic variations clustered in the antigen binding sites of HLA-Bw62 molecules. The polymerase chain reaction. Trends Genet. A comprehensive approach for typing the alleles of the HLA-B locus by automated sequencing. Detection of allo-antibodies using a sensitive antiglobulin micro-cytotoxicity test: identification of low levels of preformed antibodies in accelerated allograft rejection. Anti-HLA antibodies after solid organ transplantation.

Pre-transplant assessment of donor-reactive, HLA-specific antibodies in renal transplantation: contraindication vs. Am J Transplant. Impact of HLA class I and class II high-resolution matching on outcomes of unrelated donor bone marrow transplantation: HLA-C mismatching is associated with a strong adverse effect on transplantation outcome.

Petersdorf EW, Malkki M. Human leukocyte antigen matching in unrelated donor hematopoietic cell transplantation. Semin Hematol. Buckley RH. Transplantation immunology: organ and bone marrow. J Allergy Clin Immunol. Whitelegg A, Barber LD. The structural basis of T-cell allorecognition. Procurement and allocation of solid organs for transplantation. Evaluation of intravenous immunoglobulin as an agent to lower allosensitization and improve transplantation in highly sensitized adult patients with end-stage renal disease: report of the NIH IG02 trial.

J Am Soc Nephrol. Plasmapheresis and intravenous immune globulin provides effective rescue therapy for refractory humoral rejection and allows kidneys to be successfully transplanted into cross-match-positive recipients. Twenty-year follow-up on the effect of HLA matching on kidney transplant survival and prediction of future twenty-year survival. Transplant Proc. High survival rates of kidney transplants from spousal and living unrelated donors.

Thomas ED. Bone marrow transplantation: a review. Adult umbilical cord blood transplantation: a comprehensive review. Bone Marrow Transplant. Martin PJ. The role of donor lymphoid cells in allogeneic marrow engraftment.

Cornelissen JJ, Lowenberg B. Developments in T-cell depletion of allogeneic stem cell grafts. Curr Opin Hematol. Allogeneic marrow grafting for treatment of aplastic anemia. Marrow transplantation from related donors other than HLA-identical siblings. Marrow transplantation from HLA-matched unrelated donors for treatment of hematologic malignancies.

The National Marrow Donor Program with emphasis on the early years. Unrelated donor stem cell transplantation: the role of the National Marrow Donor Program. Oncology Williston Park ; 17 — Maximizing optimal hematopoietic stem cell donor selection from registries of unrelated adult volunteers. Effect of HLA mismatches on the outcome of hematopoietic transplants. Curr Opin Immunol. Dickinson AM, Charron D. Non-HLA immunogenetics in hematopoietic stem cell transplantation. Biol Blood Marrow Transplant.

Natural killer receptor repertoires in transplantation. Eur J Immunogenet. Lowdell MW. Natural killer cells in haematopoietic stem cell transplantation.

Transfus Med. Goulmy E. Human minor histocompatibility antigens. Alloimmunization against the MHC antigens after platelet transfusions is due to contaminating leukocytes in the platelet suspension. It appears likely that other factors, such as viral or bacterial infections and changes in other genes, also influence the development of this complex disorder.

This version of the gene is most common among people of Han Chinese or southeast Asian descent. In a process that is not well understood, the triggering drug causes immune cells called cytotoxic T cells and natural killer NK cells to release a substance called granulysin. This substance destroys cells in the skin and mucous membranes, including the lining of the mouth and the airways. The death of these cells causes severe blistering and peeling that can have life-threatening effects.

The HLA-B27 variant is associated with a group of inflammatory joint diseases related to ankylosing spondylitis. These conditions are known as spondyloarthropathies. Some of these disorders are associated with a common skin condition called psoriasis or with chronic disorders that cause inflammation of the intestinal walls inflammatory bowel disease.

One of the spondyloarthropathies, reactive arthritis, is typically triggered by bacterial infections of the gastrointestinal or genital tract. Following an infection, affected individuals may develop arthritis, back pain, and eye inflammation.

Like ankylosing spondylitis, many factors probably contribute to the development of reactive arthritis and other spondyloarthropathies. This medication slows the spread of the HIV-1 virus in the body. People with abacavir hypersensitivity often develop a fever, chills, rash, upset stomach, and other symptoms when treated with this drug.

AIDS is a disease that damages the immune system, preventing it from effectively defending the body against infections. Another version of the HLA-B gene, HLA-B53 , has been shown to help protect against severe malaria, a disease caused by a parasite that is carried by mosquitoes. The human leukocyte antigen HLA system the major histocompatibility complex [MHC] in humans is an important part of the immune system and is controlled by genes located on chromosome 6.

It encodes cell surface molecules specialized to present antigenic peptides to the T-cell receptor TCR on T cells. See also Overview of the Immune System Overview of the Immune System The immune system distinguishes self from nonself and eliminates potentially harmful nonself molecules and cells from the body.

The immune system also has the capacity to recognize and destroy Class I MHC molecules are present as transmembrane glycoproteins on the surface of all nucleated cells. Intact class I molecules consist of an alpha heavy chain bound to a beta-2 microglobulin molecule.

The heavy chain consists of 2 peptide-binding domains, an immunoglobulin Ig -like domain, and a transmembrane region with a cytoplasmic tail. These lymphocytes often have a cytotoxic function, requiring them to be capable of recognizing any infected cell. Because every nucleated cell expresses class I MHC molecules, all infected cells can act as antigen-presenting cells for CD8 T cells CD8 binds to the nonpolymorphic part of the class I heavy chain.

Class II MHC molecules are usually present only on professional antigen-presenting cells B cells, macrophages, dendritic cells, Langerhans cells , thymic epithelium, and activated but not resting T cells; most nucleated cells can be induced to express class II MHC molecules by interferon IFN -gamma. T cells reactive to class II molecules express CD4 and are often helper cells. It is the most important area in the vertebrate genome regarding infection and autoimmunity, and is essential in adaptive and innate immunity.

The HLA gene complex is located on a 3-Mbp stretch within short arm of chromosome number 6p The antigens of the HLA complex can be classified into three classes: class 1, class 2, and class 3. The likelihood of having a perfect match with someone unrelated to you is approximately 1 in , HLA complex is found on chromosome 6 in humans [ 5 ]. The alpha chain is encoded by many genes which are highly polymorphic, while beta-2 microglobulin subunit is not polymorphic and encoded by genes called beta-2 microglobulin gene.

Structure of MHC class I. Every domain is encoded by a diverse exon gene, and other genes contain domains that encode different parts leader sequences, transmembrane sequences, and cytoplasmic tail.

Antigen-binding groove of MHC class II molecules is open at both ends and the groove on class I molecules is closed at each end resulting in antigens that bind to MHC class II molecules longer about 15—24 amino acid residues long. These domains are also highly polymorphic Figure 3 [ 7 ]. The major histocompatibility complex is a highly polymorphic region in the human genome located on short arm of chromosome number 6 about genes in the region and is directly involved with the immune system.

This is due to balancing selection acting on many genes with recombination in the MHC region [ 8 ]. These genes are in association with nonimmunologic genes like noncoding RNA genes, including expressed pseudogenes.



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