ANTÍGENO LEUCOCITARIO HUMANO DE CLASE III: REVISIÓN INTEGRADORA

Autores/as

DOI:

https://doi.org/10.47820/recima21.v5i3.4891

Palabras clave:

Complejo de histocompatibilidad, Polimorfismo, Enfermedades, Salud, Inmunología, Genética

Resumen

El Antígeno Leucocitario Humano Clase III (HLA Clase III) posee polimorfismos genéticos que se correlacionan con la etiopatogenia, susceptibilidad y gravedad de las enfermedades que afectan al ser humano. Objetivo: El estudio tiene como objetivo esclarecer el papel de los polimorfismos y las acciones presentes en HLA Clase III en los síntomas y patogénesis de enfermedades crónicas, autoinmunes, inflamatorias, cancerígenas e infecciosas que afectan a la humanidad. Metodología: Se trata de una Revisión Integradora, basada en las siglas PCC e incluyendo las bases de datos Biblioteca Virtual en Salud (BVS), Capes Periódicos, Google Scholar, Embase, Medical Literature Analysis and Retrieval System Online (MEDLINE), Brazilian Bibliography of Dentistry (BBO), ScienceDirect y Scopus. Se utilizaron como descriptores los términos de interés encontrados en los Medical Subject Headings (MeSH) y en los Descriptores de Ciencias de la Salud (DeCS). Resultados: se recuperaron 56 estudios, incluidos 35 artículos de casos y controles, 3 artículos de estudios in vivo, 2 artículos de revisión de la literatura, 15 artículos de estudios de cohortes y 1 artículo de informes de casos. Los polimorfismos de HLA Clase III se deben a mutaciones aisladas y coordinadas con otros loci de genes. Conclusión: Los polimorfismos HLA Clase III pueden corroborar directa o indirectamente enfermedades que afectan a algunas poblaciones humanas.

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Biografía del autor/a

  • Luan Nascimento Mesquita

    Universidade Federal do Pará.

  • Brenda Pinto de Moraes

    Universidade da Amazônia.

  • Herika dos Santos Anijar

    Escola Superior da Amazonia.

  • Fernanda Farias de Alcântara Marchesan

    Universidade Federal do Pará.

  • Erika Vanessa Oliveira Jorge

    Universidade Federal do Pará.

  • Rebeca Fontenele Pinheiro

    Universidade do Estado do Pará.

  • Kássia Helena Silva Leitão

    Universidade do Estado do Pará.

  • Patricia Jeanne de Souza Mendonça Mattos

    Fundação Hemopa.

Referencias

ABIDA, O.; MAHFOUDH, N.; KAMMOUN, A.; GADDOUR, L.; HAKIM, F.; TOUMI, A.; MASMOUDI, A.; BEN AYED, M.; TURKI, H.; MASMOUDI, H.; MAKNI, H. Polymorphisms of HLA microsatellite marker in Tunisian pemphigus foliaceus. Human immunology, v. 74, n. 1, p. 104–109, 2013. https://doi.org/10.1016/j.humimm.2012.10.013 DOI: https://doi.org/10.1016/j.humimm.2012.10.013

AISSANI, B.; BOEHME, A. K.; WIENER, H. W.; SHRESTHA, S.; JACOBSON, L. P.; KASLOW, R. A. SNP screening of central MHC-identified HLA-DMB as a candidate susceptibility gene for HIV-related Kaposi's sarcoma. Genes and immunity, v. 15, n. 6, p. 424–429, 2014. https://doi.org/10.1038/gene.2014.42 DOI: https://doi.org/10.1038/gene.2014.42

AISSANI, B.; MARTINEZ-MAZA, O.; KASLOW, R. A.; WIENER, H. W.; BREAM, J. H.; STOSOR, V.; MARTINSON, J. J.; JACOBSON, L. P.; SHRESTHA, S. Increasing Levels of Serum Heat Shock Protein 70 Precede the Development of AIDS-Defining Non-Hodgkin Lymphoma Among Carriers of HLA-B8-DR3. Journal of acquired immune deficiency syndromes, v. 81, n. 3, p. 266–273, 2019. https://doi.org/10.1097/QAI.0000000000002027 DOI: https://doi.org/10.1097/QAI.0000000000002027

AUCKLAND, K.; MITTAL, B.; CAIRNS, B. J.; GARG, N.; KUMAR, S.; MENTZER, A. J.; KADO, J.; PERMAN, M. L.; STEER, A. C.; HILL, A. V. S.; PARKS, T. The Human Leukocyte Antigen Locus and Rheumatic Heart Disease Susceptibility in South Asians and Europeans. Scientific reports, v. 10, n. 1, 9004, 2020. https://doi.org/10.1038/s41598-020-65855-8 DOI: https://doi.org/10.1038/s41598-020-65855-8

BIELICKI, P.; MACLEOD, A. K.; DOUGLAS, N. J.; RIHA, R. L. Cytokine gene polymorphisms in obstructive sleep apnoea/hypopnoea syndrome. Sleep medicine, v. 16, n. 6, p. 792-795, 2015. https://doi.org/10.1016/j.sleep.2015.01.006 DOI: https://doi.org/10.1016/j.sleep.2015.01.006

BOIOCCHI, C.; MAGGIOLI, E.; MONTI, M. C.; ZORZETTO, M.; SINFORIANI, E.; CEREDA, C.; RICEVUTI, G.; CUCCIA, M. The Possible Involvement of HLA Class III Haplotype (RAGE, HSP70 and TNF Genes) in Alzheimer's Disease. Current Alzheimer research, v. 12, n. 10, p. 997–1005, 2015. https://doi.org/10.2174/1567205012666151027130635 DOI: https://doi.org/10.2174/1567205012666151027130635

BUSTAMANTE, M. L. B. P.; LÓPEZ, M. Á. N.; ANEIROS, J. F.; RUIZ, J. C.; LINARES, S. G.; RODRÍGUEZ, S. P.; SANTIAGO, S. A. Study of Human Leukocyte Antigen (HLA) in 13 cases of familial frontal fibrosing alopecia: CYP21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA -A*33:01 ; B*14:02; C*08:02 as a genetic marker. Australasian Journal of Dermatology, 2019. doi:10.1111/ajd.12985 DOI: https://doi.org/10.1111/ajd.12985

CARDILI, R. N.; DEGHAIDE, N. S.; MENDES-JUNIOR, C. T.; DONADI, E. A.; SOUZA, C. S. HLA-C and TNF gene polymorphisms are associated with psoriasis in Brazilian patients. International journal of dermatology, v. 55, n. 1, e16–e22, 2016. https://doi.org/10.1111/ijd.12894 DOI: https://doi.org/10.1111/ijd.12894

CHARFI, A.; MAHFOUDH, N.; KAMOUN, A.; FRIKHA, F.; DAMMAK, C.; GADDOUR, L.; HAKIM, F.; MAALEJ, L.; MALLEK, B.; KAMMOUN, I.; BAHLOUL, Z.; MAKNI, H. Association of HLA Alleles with Primary Sjögren Syndrome in the South Tunisian Population. Medical Principles and Practice: international journal of the Kuwait University, Health Science Centre, v. 29, n. 1, p. 32–38, 2020. https://doi.org/10.1159/000501896 DOI: https://doi.org/10.1159/000501896

CHENG, S.; LI, J.; LIU, W.; LIU, C.; SU, L.; LIU, X.; GUO, L.; MA, Y.; SONG, B.; LIU, J. LTA + 252A > G polymorphism is associated with risk of nasal NK/T-cell lymphoma in a Chinese population: a case-control study. BMC Cancer, v. 15, n. 480, 2015. https://doi.org/10.1186/s12885-015-1506-4 DOI: https://doi.org/10.1186/s12885-015-1506-4

CHUNG, S. A.; NITITHAM, J.; ELBOUDWAREJ, E.; QUACH, H. L.; TAYLOR, K. E.; BARCELLOS, L. F.; CRISWELL, L. A. Genome-wide assessment of differential DNA methylation associated with autoantibody production in systemic lupus erythematosus. PloS one, v. 10, n. 7, p. e0129813, 2015. https://doi.org/10.1371/journal.pone.0129813 DOI: https://doi.org/10.1371/journal.pone.0129813

CLEYNEN, I.; KONINGS, P.; ROBBERECHT, C.; LAUKENS, D.; AMININEJAD, L.; THÉÂTRE, E.; MACHIELS, K.; ARIJS, I.; RUTGEERTS, P.; LOUIS, E.; FRANCHIMONT, D.; DE VOS, M.; STEEN, K. V.; GEORGES, M.; MOREAU, Y.; VERMEESCH, J.; VERMEIRE, S. Genome-Wide Copy Number Variation Scan Identifies Complement Component C4 as Novel Susceptibility Gene for Crohn's Disease. Inflammatory Bowel Diseases, v. 22, n. 3, p. 505-515, 2016. https://doi.org/10.1097/MIB.0000000000000623 DOI: https://doi.org/10.1097/MIB.0000000000000623

CRATO, A. N.; VIDAL, L. F.; BERNARDINO, P. A.; RIBEIRO JÚNIOR, H. D. C.; ZARZAR, P. M. P. A.; PAIVA, S. M. D.; PORDEUS, I. A. Como realizar uma análise crítica de um artigo científico. Arq Odontol, v. 40, n. 1, p. 5-17, 2004. https://www.odonto.ufmg.br/revista/wp-content/uploads/sites/10/2016/06/AEO-v40-n1-arch1-2004.pdf

DENDROU, C.; PETERSEN, J.; ROSSJOHN, J.; FUGGER, L. HLA variation and disease. Nat Rev Immunol, v. 18, p. 325–339, 2018. https://doi.org/10.1038/nri.2017.143 DOI: https://doi.org/10.1038/nri.2017.143

GALIL, S. M. A.; EZZELDIN, N.; FAWZY, F.; EL-BOSHY, M. The single-nucleotide polymorphism (SNP) of tumor necrosis factor α -308G/A gene is associated with early-onset primary knee osteoarthritis in an Egyptian female population. Clinical rheumatology, v. 36, n. 11, p. 2525–2530, 2017. https://doi.org/10.1007/s10067-017-3727-1 DOI: https://doi.org/10.1007/s10067-017-3727-1

GALVÃO, M. C. B.; RICARTE, I. L. M. Revisão sistemática da literatura: conceituação, produção e publicação. Logeion: Filosofia da informação, v. 6, n. 1, p. 57-73, 2019. DOI: https://doi.org/10.21728/logeion.2019v6n1.p57-73 DOI: https://doi.org/10.21728/logeion.2019v6n1.p57-73

GÁLVEZ, A. A.; ÁVILA, G. G.; RODRÍGUEZ, M. P.; RODRÍGUEZ, O. P.; RAMÍREZ, M. N.; RAMÍREZ, I. P.; MARTÍNEZ, G. R.; LÓPEZ, M. C.; CHECA, M.; RUIZ, V.; URREA, F.; SOMMER, B.; ZÚÑIGA, J.; SELMAN, M. Analysis of heat shock protein 70 gene polymorphisms Mexican patients with idiopathic pulmonary fibrosis. BMC Pulmonary Medicine, v. 15, n. 1, p. 1-8, 2015. https://doi.org/10.1186/s12890-015-0127-7 DOI: https://doi.org/10.1186/s12890-015-0127-7

GAO, J.; TENG, J.; LIU, H.; HAN, X.; CHEN, B.; XIE, A. Association of RAGE gene polymorphisms with sporadic Parkinson's disease in Chinese Han population. Neuroscience Letters, v. 559, p. 158-162, 2014. https://doi.org/10.1016/j.neulet.2013.11.038 DOI: https://doi.org/10.1016/j.neulet.2013.11.038

GIANFRANCESCO, M. A.; STRIDH, P.; SHAO, X.; RHEAD, B.; GRAVES, J. S.; CHITNIS, T.; WALDMAN, A.; LOTZE, T.; SCHREINER, T.; BELMAN, A.; GREENBERG, B.; GUTTMAN, B. W.; AAEN, G.; TILLEMA, J. M.; HART, J.; CAILLIER, S.; NESS, J.; HARRIS, Y.; RUBIN, J.; CANDEE M.; KRUPP, L.; GORMAN, M.; BENSON, L.; RODRIGUEZ, M.; MAR, S.; KAHN, I.; ROSE, J.; ROALSTAD, S.; CASPER, T C.; SHEN, L.; QUACH, H.; QUACH, D.; HILLERT, J.; HEDSTROM, A.; OLSSON, T.; KOCKUM, I.; ALFREDSSON, L.; SCHAEFER, C.; BARCELLOS, L. F.; WAUBANT, E.; Network of Pediatric Multiple Sclerosis Centers. Genetic risk factors for pediatric-onset multiple sclerosis. Multiple Sclerosis Journal, v. 24, n. 14, p. 1825-1834, 2018. https://doi.org/10.1177/1352458517733551 DOI: https://doi.org/10.1177/1352458517733551

HACHICHA, H.; MAHFOUDH, N.; FOURATI, H.; ELLOUMI, N.; MARZOUK, S.; FEKI, S.; FAKHFAKH, R.; FRIKHA, F.; AYADI, A.; MAATOUG, A.; GADDOUR, L.; HAKIM, F.; BAHLOUL, Z.; MAKNI, H.; MASMOUDI, H.; KAMMOUN, A. HLA Class III: A susceptibility region to systemic lupus erythematosus in Tunisian population. PLOS ONE, v. 13, n. 6, p. e0198549, 2018. https://doi.org/10.1371/journal.pone.0198549 DOI: https://doi.org/10.1371/journal.pone.0198549

HRYSHCHENKO, N. V.; KIRICHENKOVA, O. P.; GORDIYK, V. V.; KRAVCHENKO, S. A.; KASHUBA, V. I. Set of STR-markers for 6p21.31 chromosomal region linkage analysis and CNV study. Biopolymers and Cell, v. 35, n. 5, p. 333-339, 2019. http://dx.doi.org/10.7124/bc.000A10 DOI: https://doi.org/10.7124/bc.000A10

JAYAKRISHNAN, R.; LAO, Q.; ADAMS, S. D.; WARD, W. W.; MERKE, D. P. Revisiting the association of HLA alleles and haplotypes with CYP21A2 mutations in a large cohort of patients with congenital adrenal hyperplasia. Gene, v. 687, p. 30–34, 2019. https://doi.org/10.1016/j.gene.2018.11.023 DOI: https://doi.org/10.1016/j.gene.2018.11.023

KAIDONIS, G.; CRAIG, J. E.; GILLIES, M. C.; ABHARY, S.; ESSEX, R. W.; CHANG, J. H.; PAL, B.; PEFKIANAKI, M.; DANIELL, M.; LAKE, S.; PETROVSKY, N.; BURDON, K. P. Promoter polymorphism at the tumour necrosis factor/lymphotoxin-alpha locus is associated with type of diabetes but not with susceptibility to sight-threatening diabetic retinopathy. Diabetes & vascular disease research, v. 13, n. 2, p. 164–167, 2016. https://doi.org/10.1177/1479164115616902 DOI: https://doi.org/10.1177/1479164115616902

KALLIO, K. E.; MARCHESANI, M.; VLACHOPOULOU, E.; MÄNTYLÄ, P.; PAJU, S.; BUHLIN, K.; SUOMINEN, A. L.; CONTRERAS, J.; KNUUTTILA, M.; HERNANDEZ, M.; HUUMONEN, S.; NIEMINEN, M. S.; PEROLA, M.; SINISALO, J.; LOKKI, M. L.; PUSSINEN, P. J. Genetic variation on the BAT1-NFKBIL1-LTA region of major histocompatibility complex class III associates with periodontitis. Infection and Immunity, v. 82, n. 5, p. 1939-1948, 2014. https://doi.org/10.1128%2FIAI.01681-13 DOI: https://doi.org/10.1128/IAI.01681-13

KIKUCHI, K.; ABE, S.; KODAIRA, K.; YUKAWA, T.; HOZAWA, S.; MOCHIZUKI, H.; KUROSAWA, M. Heat shock protein 70 gene polymorphisms in Japanese patients with aspirin-exacerbated respiratory disease. Journal of investigative medicine: the official publication of the American Federation for Clinical Research, v. 61, n. 4, p. 708–714, 2013. https://doi.org/10.2310/JIM.0b013e3182857d6c DOI: https://doi.org/10.2310/JIM.0b013e3182857d6c

KOLHO, K. L.; PAAKKANEN, R.; LEPISTÖ, A.; WENNERSTÖM, A.; MERI, S.; LOKKI, M. L. Novel Associations Between Major Histocompatibility Complex and Pediatric-onset Inflammatory Bowel Disease. Journal of pediatric gastroenterology and nutrition, v. 62, n. 4, p. 567–572, 2016. https://doi.org/10.1097/mpg.0000000000000984 DOI: https://doi.org/10.1097/MPG.0000000000000984

KOTHARI, N.; BOGRA, J.; ABBAS, H.; KOHLI, M.; MALIK, A.; KOTHARI, D.; SRIVASTAVA, S.; SINGH, P. K. Tumor necrosis factor gene polymorphism results in high TNF level in sepsis and septic shock. Cytokine, v. 61, n. 2, p. 676–681, 2013. https://doi.org/10.1016/j.cyto.2012.11.016 DOI: https://doi.org/10.1016/j.cyto.2012.11.016

KREUZ, J. I.; CARLSSON, J. C. A.; LEONARD, D.; ALEXSSON, A.; NORDMARK, G.; ELORANTA, M. L.; RANTAPÄÄ, S. D.; BENGTSSON, A. A.; JÖNSEN, A.; PADYUKOV, L.; GUNNARSSON, I.; SVENUNGSSON, E.; SJÖWALL, C.; RÖNNBLOM, L.; SYVÄNEN, A. C.; SANDLING, J. K. DNA methylation mapping identifies gene regulatory effects in patients with systemic lupus erythematosus. Annals of the rheumatic diseases, v. 77, n. 5, p. 736–743, 2018. https://doi.org/10.1136/annrheumdis2017-212379 DOI: https://doi.org/10.1136/annrheumdis-2017-212379

LIU, J.; LIU, J.; SONG, B.; WANG, T.; LIU, Y.; HAO, J.; YU, J. Genetic variations in CTLA-4, TNF-α, and LTA and susceptibility to T-cell lymphoma in a Chinese population. Cancer epidemiology, v. 37, n. 6, p. 930-934, 2013. DOI: 10.1016/j.canep.2013.08.011 DOI: https://doi.org/10.1016/j.canep.2013.08.011

LIU, L.; CHEN, J.; LI, J.; YANG, Y.; ZENG, X.; TIAN, X. Whole Exome Sequencing Revealed Variants That Predict Pulmonary Artery Involvement in Patients with Takayasu Arteritis. J Inflamm Res., v. 15, p. 4817-4831, 2022. https://doi.org/10.2147/JIR.S377402 DOI: https://doi.org/10.2147/JIR.S377402

LIUKKONEN, J.; GÜRSOY, U. K.; KÖNÖNEN, E.; GÜRSOY, M.; METSO, J.; SALMINEN, A.; KOPRA, E.; JAUHIAINEN, M.; MÄNTYLÄ, P.; BUHLIN, K.; PAJU, S.; SORSA, T.; NIEMINEN, M. S.; LOKKI, M.-L.; SINISALO, J.; PUSSINEN, P. J. Salivary biomarkers in association with periodontal parameters and the periodontitis risk haplotype. Innate Immunity, v. 24, n. 7, p. 439-447, 2018. doi:10.1177/1753425918796207 DOI: https://doi.org/10.1177/1753425918796207

LONEY, P. L.; CHAMBERS, L. W.; BENNETT, K. J.; ROBERTS, J. G.; STRATFORD, P. W. Critical appraisal of the health research literature: prevalence or incidence of a health problem. Chronic diseases in Canada, v. 19, n. 4, p. 170–176, 1998. https://www.researchgate.net/publication/13259110_Critical_Appraisal_of_the_Health_Research_Literature_Prevalence_or_Incidence_of_a_Health_Problem

MAGGIOLI, E.; BOIOCCHI, C.; ZORZETTO, M.; MANNARINO, S.; BOSSI, G.; CUCCIA, M. HLA class III genes involvement in Kawasaki disease: a case-control study in Caucasian population. International journal of immunogenetics, v. 41, n. 1, p. 44–53, 2014. https://doi.org/10.1111/iji.12077 DOI: https://doi.org/10.1111/iji.12077

MAGGIOLI, E.; BOIOCCHI, C.; ZORZETTO, M.; SINFORIANI, E.; CEREDA, C.; RICEVUTI, G.; CUCCIA, M. The human leukocyte antigen class III haplotype approach: new insight in Alzheimer's disease inflammation hypothesis. Current Alzheimer research, v. 10, n. 10, p. 1047–1056, 2013. https://doi.org/10.2174/15672050113106660169 DOI: https://doi.org/10.2174/15672050113106660169

MANOLOVA, I.; IVANOVA, M.; STOILOV, R.; RASHKOV, R.; STANILOVA, S. Association of single nucleotide polymorphism at position− 308 of the tumor necrosis factor-alpha gene with ankylosing spondylitis and rheumatoid arthritis. Biotechnology & Biotechnological Equipment, v. 28, n. 6, p. 1108-1114, 2014. http://dx.doi.org/10.1080/13102818.2014.972147 DOI: https://doi.org/10.1080/13102818.2014.972147

MENDES, K. D. S.; SILVEIRA, R. C. D. C. P.; GALVÃO, C. M. Revisão integrativa: método de pesquisa para a incorporação de evidências na saúde e na enfermagem. Texto & contexto-enfermagem, v. 17, p. 758-764, 2008. https://doi.org/10.1590/S0104-07072008000400018 DOI: https://doi.org/10.1590/S0104-07072008000400018

MENDONÇA, V. R.; SOUZA, L. C.; GARCIA, G. C.; MAGALHÃES, B. M.; LACERDA, M. V.; ANDRADE, B. B.; GONÇALVES, M. S.; NETTO, M. B. DDX39B (BAT1), TNF and IL6 gene polymorphisms and association with clinical outcomes of patients with Plasmodium vivax malaria. Malaria journal, v. 13, n. 1, p. 1-13, 2014. https://doi.org/10.1186/1475-2875-13-278 DOI: https://doi.org/10.1186/1475-2875-13-278

MITSUNAGA, S.; HOSOMICHI, K.; OKUDAIRA, Y.; NAKAOKA, H.; KUNII, N.; SUZUKI, Y.; KUWANA, M.; SATO, S.; KANEKO, Y.; HOMMA, Y.; KASHIWASE, K.; AZUMA, F.; KULSKI, J. K.; INOUE, I.; INOKO, H. Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2. Journal of human genetics, v. 58, n. 4, p. 210-215, 2013. https://doi.org/10.1038/jhg.2013.2 DOI: https://doi.org/10.1038/jhg.2013.2

MOTAWI, T. K.; EL-MARAGHY, S. A.; SHARAF, S. A.; SAID, S. E. Association of CARD10 rs6000782 and TNF rs1799724 variants with paediatric-onset autoimmune hepatitis. Journal of advanced research, v. 15, p. 103–110, 2019. https://doi.org/10.1016/j.jare.2018.10.001 DOI: https://doi.org/10.1016/j.jare.2018.10.001

MOYER, A. M.; HASHMI, S. K.; KRONING, C.; DE GOEY, S. R.; PATNAIK, M.; LITZOW, M.; GASTINEAU, D. A.; HOGAN, W. J.; JACOB, E. K.; KREUTER, J. D.; WAKEFIELD, L. L.; GANDHI, M. J. Does matching for SNPs in the MHC gamma block in 10/10 HLA-matched unrelated donor-recipient pairs undergoing allogeneic stem cell transplant improve outcomes?. Human immunology, v. 79, n. 7, p. 532–536, 2018. https://doi.org/10.1016/j.humimm.2018.04.008 DOI: https://doi.org/10.1016/j.humimm.2018.04.008

MURDACA, G.; GULLI, R.; SPANÒ, F.; LANTIERI, F.; BURLANDO, M.; PARODI, A.; MANDICH, P.; PUPPO, F. TNF-α gene polymorphisms: association with disease susceptibility and response to anti-TNF-α treatment in psoriatic arthritis. The Journal of investigative dermatology, v. 134, n. 10, p. 2503–2509, 2014. https://doi.org/10.1038/jid.2014.123 DOI: https://doi.org/10.1038/jid.2014.123

MURDACA, G.; PUPPO, F. Tumor necrosis factor (TNF)-α gene+ 489 polymorphisms: association with psoriatic arthritis. Journal of Biological Research-Bollettino della Società Italiana di Biologia Sperimentale, v. 86, n. 1, 2013. https://doi.org/10.4081/jbr.2013.3674 DOI: https://doi.org/10.4081/jbr.2013.3674

NÆSS, S.; LIE, B. A.; MELUM, E.; OLSSON, M.; HOV, J. R.; CROUCHER, P. J.; HAMPE, J.; THORSBY, E.; BERGQUIST, A.; TRAHERNE, J. A.; SCHRUMPF, E.; BOBERG, K. M.; SCHREIBER, S.; FRANKE, A.; KARLSEN, T. H. Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population. PloS one, v. 9, n. 12, p. e114486, 2014. https://doi.org/10.1371/journal.pone.0114486 DOI: https://doi.org/10.1371/journal.pone.0114486

NAITO, T.; SATAKE, W.; OGAWA, K.; SUZUKI, K.; HIRATA, J.; FOO, J. N.; TAN, E. K.; TODA, T.; OKADA, Y. Trans-Ethnic Fine-Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease. Movement disorders: official journal of the Movement Disorder Society, v. 36, n. 8, p. 1805–1814, 2021. https://doi.org/10.1002/mds.28583 DOI: https://doi.org/10.1002/mds.28583

PAGE, M. J.; MCKENZIE, J. E.; BOSSUYT, P. M.; BOUTRON, I.; HOFFMANN, T. C.; MULROW, C. D.; SHAMSEER, L.; TETZLAF, J. M.; AKL, E. A.; BRENNAN, S. E.; CHOU, R.; GLANVILLE, J.; GRIMSHAW, J. M.; HRÓBJARTSSON, A.; LALU, M. M.; LI, T.; LODER, E. W.; WILSON, E. M.; MCDONALD, S.; MCGUINNESS, L. A.; STEWART, L. A.; THOMAS, J.; TRICCO, A. C.; WELCH, V. A.; WHITING, P.; MOHER, D. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ, n. 71, 2021. doi:10.1136/bmj.n71 DOI: https://doi.org/10.1136/bmj.n71

PENG, Y.; LI, L. J. TNF-α-308G/A polymorphism associated with TNF-α protein expression in patients with diabetic nephropathy. International journal of clinical and experimental pathology, v. 8, n. 3, p. 3127–3131, 2015.

PETERS, M. D. J.; GODFREY, C.; MCINERNEY, P.; MUNN, Z.; TRICCO, A. C.; KHALIL, H.; Revisões do escopo (Versão 2020). In: AROMATARIS, E.; MUNN, Z (Editores). JBI Manual for Evidence Synthesis. [S. l]: JBI, 2020. https://doi.org/10.46658/JBIMES-20-12 DOI: https://doi.org/10.46658/JBIMES-20-12

PIRAS, I. S.; ANGIUS, A.; ANDREANI, M.; TESTI, M.; LUCARELLI, G.; FLORIS, M.; MARKTEL, S.; CICERI, F.; NASA, G. L.; FLEISCHHAUER, K.; RONCAROLO, M. G.; BULFONE, A.; GREGORI, S.; BACCHETTA, R. BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT. Bone Marrow Transplantation, v. 49, n. 11, p. 1400–1404, 2014. doi:10.1038/bmt.2014.177 DOI: https://doi.org/10.1038/bmt.2014.177

SCALE, N. O. Q. A. Case control studies. [S. l.: s. n.], 2011. Disponível em: https://www.ohri.ca/programs/clinical_epidemiology/nosgen.pdf

SCHOTT, G.; BLANCO, M. A. G MHC Class III RNA Binding Proteins and Immunity. RNA biology, v. 18, n. 5, p. 640–646, 2021. https://doi.org/10.1080/15476286.2020.1860388 DOI: https://doi.org/10.1080/15476286.2020.1860388

SELDIN, M. F.; ALKHAIRY, O. K.; LEE, A. T.; LAMB, J. A.; SUSSMAN, J.; MATELL, R. P.; PIEHL, F.; VERSCHUUREN, J. J. G. M.; PRUSZCZYK, A. K.; SZCZUDLIK, P.; MCKEE, D.; MANIAOL, A. H.; HARBO, H. F.; LIE, B. A.; MELMS, A.; GARCHON, H. J.; WILLCOX, N.; GREGERSEN, P. K.; HAMMARSTROM, L. Genome-wide association study of late-onset myasthenia gravis: Confirmation of TNFRSF11A and identification of ZBTB10 and three distinct HLA associations. Molecular Medicine, v. 21, n. 1, p. 769-781, 2015. https://doi.org/10.2119/molmed.2015.00232 DOI: https://doi.org/10.2119/molmed.2015.00232

SHAKER, O. G.; SADIK, N. A.; EL-HAMID, N. A. Impact of single nucleotide polymorphism in tumor necrosis factor-α gene 308G/A in Egyptian asthmatic children and wheezing infants. Human immunology, v. 74, n. 6, p. 796–802, 2013. https://doi.org/10.1016/j.humimm.2013.01.004 DOI: https://doi.org/10.1016/j.humimm.2013.01.004

SILVA, G. A. V.; RAMASAWMY, R.; BOECHAT, A. L.; MORAIS, A. C.; CARVALHO, B. K. S.; SOUSA, K. B. A.; SOUZA, V. C.; CUNHA, M. G. S.; BARLETTA, R. H. N.; SANTOS, M. P.; NAVECA, F. G. Association of TNF− 1031 C/C as a potential protection marker for leprosy development in Amazonas state patients, Brazil. Human Immunology, v. 76, n. 2-3, p. 137-141, 2015. 10.1016/j.humimm.2015.01.011 DOI: https://doi.org/10.1016/j.humimm.2015.01.011

SOUSA, L. M. M.; FIRMINO, C. F.; VIEIRA, C. M. A. M.; SEVERINO, S. S. P.; PESTANA, H. C. F. C. Revisões da literatura científica: tipos, métodos e aplicações em enfermagem. Revista Portuguesa de Enfermagem de Reabilitação, v. 1, n. 1, p. 45-54, 2018. https://doi.org/10.33194/rper.2018.v1.n1.07.4391 DOI: https://doi.org/10.33194/rper.2018.v1.n1.07.4391

SOUSA, L. M. M.; VIEIRA, C. M. A. M.; SEVERINO, S. S. P.; ANTUNES, A. V. A metodologia de revisão integrativa da literatura em enfermagem. Revista Investigação Enfermagem, n. 21, nov. 2017.

SU, S.; CHIEN, M.; LIN, C.; CHEN, M.; YANG, S. RAGE gene polymorphism and environmental factor in the risk of oral cancer. Journal of dental research, v. 94, n. 3, p. 403–411, 2015. https://doi.org/10.1177/0022034514566215 DOI: https://doi.org/10.1177/0022034514566215

TOUMI, A.; ABIDA, O.; BEN-AYED, M.; MASMOUDI, A.; TURKI, H.; MASMOUDI, H. Is there any relationship between polymorphism of Heat Shock Protein 70 genes and Pemphigus foliaceus?. Immunology letters, v. 164, n. 2, p. 94–99, 2015. https://doi.org/10.1016/j.imlet.2015.01.006 DOI: https://doi.org/10.1016/j.imlet.2015.01.006

TROSHINA, E. A.; YUKINA, M. Y.; NURALIEVA, N. F.; MOKRYSHEVA, N. G. The role of HLA genes: from autoimmune diseases to COVID-19. Problemy endokrinologii, v. 66, n. 4, p. 9–15, 2020. https://doi.org/10.14341/probl12470 DOI: https://doi.org/10.14341/probl12470

TUMER, G.; SIMPSON, B.; ROBERTS, T. K. Genetics, Human Major Histocompatibility Complex (MHC). [S. l.: s. n.], 2019. https://www.ncbi.nlm.nih.gov/books/NBK538218/

VALENCIA, R. F.; CAMARENA, Á.; PINEDA, C. L.; MONTAÑO, M.; JUÁREZ, A.; ROLDÁN, I. B.; RUBIO, G. P.; HERNÁNDEZ, J. M. R.; PARÁMO, I.; VEJA, A.; GRANADOS, J.; ZÚÑIGA, J.; SELMAN, M. Genetic susceptibility to multicase hypersensitivity pneumonitis is associated with the TNF-238 GG genotype of the promoter region and HLA-DRB1* 04 bearing HLA haplotypes. Respiratory medicine, v. 108, n. 1, p. 211-217, 2014. http://dx.doi.org/10.1016/j.rmed.2013.11.004 DOI: https://doi.org/10.1016/j.rmed.2013.11.004

WEIDLE, U. H.; ROHWEDDER, I.; BIRZELE, F.; WEISS, E. H.; SCHILLER, C. LST1: A multifunctional gene encoded in the MHC class III region. Immunobiology, v. 223, n. 11, p. 699–708, 2018. https://doi.org/10.1016/j.imbio.2018.07.018 DOI: https://doi.org/10.1016/j.imbio.2018.07.018

WOLIN, A.; LAHTELA, E. L.; ANTTILA, V.; PETREK, M.; GRUNEWALD, J.; VAN MOORSEL, C. H. M.; EKLUND, A.; GRUTTERS, J. C.; KOLEK, V.; MRAZEK, F.; KISHORE, A.; PADYUKOV, L.; PIETINALHO, A.; RONNINGER, M.; SEPPÄNEN, M.; SELROOS, O.; LOKKI, M-L. SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility—A Joint Analysis in Four European Populations. Front. Immunol., v. 8, p. 422, 2017. doi: 10.3389/fimmu.2017.00422 DOI: https://doi.org/10.3389/fimmu.2017.00422

YANG, S. Y.; HAYER, K. E.; FAZELINIA, H.; SPRUCE, L. A.; ASNANI, M.; BLACK, K. L.; NAQVI, A. S.; PILLAI, V.; BARASH, Y.; ELENITOBA-JOHNSON, K. S. J.; THOMAS-TIKHONENKO, A. FBXW7β isoform drives transcriptional activation of a proinflammatory TNF cluster in normal and malignant pro-B cells. Blood advances, 2022b. https://doi.org/10.1182/bloodadvances.2022007910

YANG, S. Y.; HAYER, K. E.; FAZELINIA, H.; SPRUCE, L. A.; ASNANI, M.; BLACK, K. L.; NAQVI, A. S.; PILLAI, V.; BARASH, Y.; ELENITOBA, K. S. J. J.; TIKHONENKO, A. T. FBXW7β isoform drives transcriptional activation of the proinflammatory TNF cluster in human pro-B cells. Blood advances, 2022a. https://doi.org/10.1182/bloodadvances.2022007910 DOI: https://doi.org/10.1101/2022.04.24.489313

YANG, Y. H.; LIU, Y. Q.; ZHANG, L.; LI, H.; LI, X. B.; OUYANG, Q.; ZHU, G. Y. Genetic polymorphisms of the TNF-α-308G/A are associated with metabolic syndrome in asthmatic patients from Hebei province, China. International Journal of Clinical and Experimental Pathology, v. 8, n. 10, p. 13739, 2015. PMID: 26722602; PMCID: PMC4680547.

YOSHIDA, W. B. Redação do relato de caso. Jornal Vascular Brasileiro, v. 6, p. 112-113, 2007. https://doi.org/10.1590/S1677-54492007000200004 DOI: https://doi.org/10.1590/S1677-54492007000200004

YUCESOY, B.; TALZHANOV, Y.; MICHAEL BARMADA, M.; JOHNSON, V. J.; KASHON, M. L.; BARON, E.; WILSON, N. W.; FRYE, B., WANG, W.; FLUHARTY, K.; GHARIB, R.; MEADE, J., GERMOLEC, D.; LUSTER, M. I.; NEDOROST, S. Association of MHC region SNPs with irritant susceptibility in healthcare workers. Journal of immunotoxicology, v. 13, n. 5, p. 738-744, 2016. https://doi.org/10.3109/1547691X.2016.1173135 DOI: https://doi.org/10.3109/1547691X.2016.1173135

YUE, H.; HAN, W.; SHENG, L. Association of pro-inflammatory cytokines gene polymorphisms with Alzheimer’s disease susceptibility in the Han Chinese population. Int J Clin Exp Med, v. 10, n. 3, p. 5422-28, 2017. https://e-century.us/files/ijcem/10/3/ijcem0023397.pdf

ZHOU, D.; RUDNICKI, M.; CHUA, G. T.; LAWRANCE, S. K.; ZHOU, B.; DREW, J. L.; BARBAR-SMILEY, F.; ARMSTRONG, T. K.; HILT, M. E.; BIRMINGHAM, D. J.; PASSLER, W.; AULETTA, J. J.; BOWDEN, S. A.; HOFFMAN, R. P.; WU, Y. L.; JARJOUR, W. N.; MOK, C. C.; ARDOIN, S. P.; LAU, Y. L.; YU, C. Y. Human Complement C4B Allotypes and Deficiencies in Selected Cases With Autoimmune Diseases. Frontiers in immunology, v. 12, p. 739430, 2021. https://doi.org/10.3389/fimmu.2021.739430 DOI: https://doi.org/10.3389/fimmu.2021.739430

ZORZETTO, M.; DATTURI, F.; DIVIZIA, L.; PISTONO, C.; CAMPO, I.; DE SILVESTRI, A.; CUCCIA, M.; RICEVUTI, G. Complement C4A and C4B Gene Copy Number Study in Alzheimer's Disease Patients. Current Alzheimer research, v. 14, n. 3, p. 303–308, 2017. https://doi.org/10.2174/1567205013666161013091934 DOI: https://doi.org/10.2174/1567205013666161013091934

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04/03/2024

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ANTÍGENO LEUCOCITARIO HUMANO DE CLASE III: REVISIÓN INTEGRADORA. (2024). RECIMA21 - Revista Científica Multidisciplinar - ISSN 2675-6218, 5(3), e534891. https://doi.org/10.47820/recima21.v5i3.4891