[Home ] [Archive]   [ فارسی ]  
:: Main :: About us :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
High Institute for Research and Education in Transfusion Medicine::
Journal Information::
Articles archive::
For Authors::
For Reviewers::
Submission::
Contact us::
Site Facilities::
Commitment letter::
Ethics & Permissions::
::
Search in website

Advanced Search
..
Receive site information
Enter your Email in the following box to receive the site news and information.
..
Indexing
                        
..
:: Volume 20, Issue 4 (Winter 2023) ::
Sci J Iran Blood Transfus Organ 2023, 20(4): 267-275 Back to browse issues page
Association of HLA-DR polymorphisms and Febrile Non-Hemolytic Transfusion Reaction in multi-transfused thalassemia patients
Z. Tasbiti , M.S. Dadashi , A. Chegini , M. Zadsar *
Keywords: Febrile Non-Hemolytic Transfusion Reaction, Blood Transfusion, Polymorphism (Genetics), HLA-DR, Thalassemia
Full-Text [PDF 426 kb]   (457 Downloads)     |   Abstract (HTML)  (1080 Views)
Type of Study: Research | Subject: Blood transfusion medicine
Published: 2023/12/31
Full-Text:   (238 Views)



Sci J Iran Blood Transfus Organ 2023;20 (4): 267-275
Original Article
 
Association of HLA-DR polymorphisms and Febrile

Non-Hemolytic Transfusion Reaction in multi-transfused
thalassemia patients

Tasbiti Z.1, Dadashi M.S.1, Chegini A.1, Zadsar M.1


1Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran


Abstract
Background and Objectives
β-thalassemia patients need regular blood. Regular blood transfusion has side effects. The most common of which is FNHTR. One of the causes of FNHTR is the antibody production against HLA-II antigens. HLA polymorphism vary in different communities and may affect the susceptibility or resistance to FNHTR. In this study, the relationship between HLA-DR polymorphisms and development of FNHTR in multi-transfused thalassemia patients in Tehran province was investigated.

Materials and Methods
In this cross-sectional study, 88 β-thalassemia major and intermediate patients with average age 38.63 ± 11.28 with 35 being male (39.8%) and 53 female (60.2%) were enrolled and for better results, 70 thalassemia patients with FNHTR were compared with 18 thalassemia patients without FNHTR. HLA-DR genotype was investigated by PCR-SSP method. Data were analyzed by chi-squared and pearson test.

Results
The results of PCR-SSP showed that HLA-DRB1*11 allele had the highest prevalence (26.7%) in the total study population. No statistically significant correlation between HLA-DR alleles and development of FNHTR was observed. Although HLA-DRB1*10 as a possible genetic marker may play a role in protecting against FNHTR (p = 0.049).

Conclusions 
In this study, no significant association between HLA-DR allele frequency and FNHTR was found. Although alleles HLA-DRB1*03, HLA-DRB1*10, HLA-DRB1*13 and HLA-DRB1*16 have higher prevalence in the no FNHTR group, but only in the case of HLA-DRB1*10 this relationship was significant and was considered as possible genetic markers against development of FNHTR. Further studies investigating HLA-II allelic levels in larger populations may provide more deep data on this association.

Key words: Febrile Non-Hemolytic Transfusion Reaction, Blood Transfusion, Polymorphism (Genetics), HLA-DR, Thalassemia



Received:  9 Oct 2023
Accepted: 4 Nov 2023



Correspondence: Zadsar M., MD. Specialist in Infectious Diseases. Associate Professor of Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine.
P.O.Box: 14665-1157, Tehran, Iran. Tel: (+9821) 88621248; Fax: (+9821) 88601555
E-mail: maryam.zad@gmail.com
References:
  1.            Kumar P, Thapliyal R, Coshic P, Chatterjee K. Retrospective evaluation of adverse transfusion reactions following blood product transfusion from a tertiary care hospital: A preliminary step towards hemovigilance. Asian J Transfus Sci 2013; 7(2): 109-15.
  2.            Delaney M, Wendel S, Bercovitz RS, Cid J, Cohn C, Dunbar NM, et al. Transfusion reactions: prevention, diagnosis, and treatment. Lancet 2016; 388(10061): 2825-36.
  3.            Wang H, Ren D, Sun H, Liu J. Research progress on febrile non-hemolytic transfusion reaction: a narrative review. Ann Transl Med 2022; 10(24): 1401.
  4.            Klein J, Sato A. The HLA system. N Engl J Med 2000; 343(10): 702-9.
  5.            Jones EY, Fugger L, Strominger JL, Siebold C. MHC class II proteins and disease: a structural perspective. Nature Reviews Immunology 2006; 6(4): 271-82.
  6.            Campbell-Lee SA, Kittles RA. Red blood cell alloimmunization in sickle cell disease: listen to your ancestors. Transfus Med Hemother 2014; 41(6): 431-5.
  7.            Andersson G. Evolution of the human HLA-DR region. Front Biosci 1998; 3(4): d739-45.
  8.            Rodrigues C, Sell A, Guelsin G, Higa T, Pagliarini e Silva S, Macedo L, et al. HLA polymorphisms and risk of red blood cell alloimmunisation in polytransfused patients with sickle cell anaemia. Transfus Med 2017; 27(6): 437-43.
  9. Ebrahimi M, Dayer D, Jalalifar MA, Keikhaei B, Tahan Nejad Asadi Z. Association between HLA-DRB1* 01 and HLA-DRB1* 15 with alloimmunisation in transfusion-dependent patients with thalassaemia. Transfus Med 2020; 30(4): 275-80.
  10. Farjadian S, Naruse T, Kawata H, Ghaderi A, Bahram S, Inoko H. Molecular analysis of HLA allele frequencies and haplotypes in Baloch of Iran compared with related populations of Pakistan. Tissue Antigens 2004; 64(5): 581-7.
  11.            Medhasi S, Chantratita N. Human Leukocyte Antigen (HLA) System: Genetics and Association with Bacterial and Viral Infections. J Immunol Res 2022; 2022: 9710376.
  12.            Li D, Sun K, Zhao Y, Lin A, Li S, Jiang Y, Feng J. Polymorphism in the major histocompatibility complex (MHC class II B) genes of the Rufous-backed Bunting (Emberiza jankowskii).  PeerJ 2017; 5: e2917.
  13.            Simmonds M, Gough S. The HLA region and autoimmune disease: associations and mechanisms of action. Curr  Genomics 2007; 8(7): 453-65.
  14.            Wang F, Huang S, Gao R, Zhou Y, Lai C, Li Z, et al. Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility. Cell Discov 2020; 6(1): 83.
  15.            Anzurez A, Naka I, Miki S, Nakayama-Hosoya K, Isshiki M, Watanabe Y, et al. Association of HLA-DRB1* 09: 01 with severe COVID-19. HLA 2021; 98(1): 37-42.
  16.            Dadashi M, Ostadali M, Mohammadi S, Azarkeivan A, Zadsar M. Major histocompatibility complex (MHC) antigens polymorphism and alloimmunization study in thalassemia patients with febrile non-hemolytic transfusion reaction (FNHTR). Transfus Clin Biol 2023; 30(2): 205-11.
  17.            Abedini F, Rahmanian N, Heidari Z, Feizi A, Sherkat R, Rezaei M. Diversity of HLA class I and class II alleles in Iran populations: Systematic review and Meta-Analaysis. Transplant Immunol 2021; 69: 101472.
  18.            Dehghani  Firouzabadi  F,   Salimi   J,   Amirzargar   A, Dehghani Firouzabadi M, Arbabi H, Mousavizadeh SM, Izadpanah K. Human leukocyte antigen class I (A, B) and class II (DRB1) allele and haplotype frequencies in Iranian patients with Buerger's disease. Immun Inflamm Dis 2020; 8(3): 434-40.
  19. Nikbin B, Nicknam MH, Hadinedoushan H, Ansaripour B, Moradi B, Yekaninejad M, et al. Human leukocyte antigen (HLA) class I and II polymorphism in Iranian healthy population from Yazd Province. Iran J Allergy Asthma Immunol 2017; 16(1): 1-13.
  20.            Arab M, Pourpak Z, Mohammadian S, Zare A, Shakiba Y, Shokouhi Shoormasti R, et al. The Frequency of Human Leukocyte Antigen Class I and II Alleles and the Relationship Between Haplotypes in Gilaks Population of Iran. Immunoregulation 2019; 2(1): 57-66.
  21.            Esmaeili  A,  Rabe  SZT,   Mahmoudi   M,   Rastin   M. Frequencies of HLA-A, B and DRB1 alleles in a large normal population living in the city of Mashhad, Northeastern Iran. Iran J Basic Med Sci 2017; 20(8): 940.
  22.            Thomsen C, Steffensen R, Nielsen H, Kolte A, Krog M, Egerup P, et al. HLA-DRB1 polymorphism in recurrent pregnancy loss: New evidence for an association to HLA-DRB1* 07. J Reprod Immunol 2021; 145: 103308.
  23.            Jazairi B, Khansaa I, Ikhtiar A, Murad H. Frequency of HLA-DRB1 and HLA-DQB1 alleles and haplotype association in Syrian population. Immunol Invest 2016; 45(2): 172-9.
  24.            Pedron B, Yakouben K, Adjaoud D, Auvrignon A, Landman J, Guerin V, et al. Listing of common HLA alleles and haplotypes based on the study of 356 families residing in the Paris, France, area: implications for unrelated hematopoietic stem cell donor selection. Hum Immunol 2005; 66(6): 720-30.
Send email to the article author

Add your comments about this article
Your username or Email:

CAPTCHA


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Tasbiti Z, Dadashi M, Chegini A, Zadsar M. Association of HLA-DR polymorphisms and Febrile Non-Hemolytic Transfusion Reaction in multi-transfused thalassemia patients. Sci J Iran Blood Transfus Organ 2023; 20 (4) :267-275
URL: http://bloodjournal.ir/article-1-1512-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 20, Issue 4 (Winter 2023) Back to browse issues page
فصلنامه پژوهشی خون Scientific Journal of Iran Blood Transfus Organ
The Scientific Journal of Iranian Blood Transfusion Organization - Copyright 2006 by IBTO
Persian site map - English site map - Created in 0.21 seconds with 39 queries by YEKTAWEB 4704