HLA Alloantibodies in Multiparous Women at Abidjan
N’guessan Koffi1, Akre Dagra Paul2, Dasse Sery Romuald1, Gobey Richard Arthur2, Fizet Dominique3, Seka Seka Joseph2, Sombo Mambo François1
1Department of Immunology-Hematology and Cancerology, Felix Houphouët Boigny University, Abidjan, Ivory Coast
2Department of Immunology, Allassane Ouattara University, Bouake, Ivory Coast
3Department of Cellular Immunology, French Blood Agency, Bordeaux, France
To cite this article:
N’guessan Koffi, Akre Dagra Paul, Dasse Sery Romuald, Gobey Richard Arthur, Fizet Dominique, Seka Seka Joseph, Sombo Mambo François. HLA Alloantibodies in Multiparous Women at Abidjan. International Journal of Immunology. Vol. 4, No. 6, 2016, pp. 64-67. doi: 10.11648/j.iji.20160406.13
Received: October 4, 2016; Accepted: November 23, 2016; Published: December 29, 2016
Abstract: Serum of multiparous women can contain HLA polyclonal antibodies which can be used as reagents for serological typing of HLA class I and class II. The aim of this study was to investigate an alloimmunization of multiparous women and to identify HLA polyclonal antibodies which could be useful as laboratory reagents in view of the future HLA unit of the Department of Immunology at Abidjan. In an experimental and analytic study, we screened HLA antibodies using microlymphocytotoxicity test on sera of 121 multiparous women aged from 18 to 70 years old, in apparent good health, transfused or no-transfused and with at least two parities. 37.19% of the multiparous women were alloimmunized. 13 women were sensitized to HLA class I, 18 to HLA class II and 14 were both sensitized to class I and class II. Specificity of the screened antibodies was identified at 17.78%. HLA-B7 specificity (Class I) was 37.5% and class II specificity (HLA-DR4, DR7, DR13, DR13+14, DRw52) was 62.5%. Specificity was evaluated by the correlation coefficient. For class I specificity correlation coefficients were ranged from 0.79 to 1, while for class II specificities, correlation coefficients were ranged from 0.54 to 0.9. Screening of HLA antibodies on multiparous women at Abidjan was positive and specificities were determined. This enabled authors to the possibility of using multiparous women sera as a source of production of polyclonal antibodies for serological HLA typing in the HLA unit of the Department of Immunology at Abidjan.
Keywords: HLA Alloimmunization, Multiparous Women, Microlymphocytotoxicity, Ivory Coast
The human leukocyte antigen (HLA) system represents a family of polymorphic cell surface molecules involved in the presentation of antigen to T cells and thus play a central role in the induction and regulation of immune responses [1,2]. Specific HLA antibodies can be produced in any situation that exposes the host to the HLA alloantigen including pregnancy, transplantation transfusion and planned vaccination . Anti-HLA antibodies can be identified in approximately 20% of pregnant women . Multiparous women can be a source of producing HLA antibodies. The production, typing and identification of HLA antibodies are part of the routine laboratory tests performed for blood donors in developed countries . Technological advances in the health sector of our country and organ transplant prospects dictate that we can routinely perform the serological typing of HLA antigens, hence the need of anti-HLA specific antibody. Serum of multiparous women may contain anti-HLA polyclonal antibodies, which can be used as reagents for serological typing of HLA class I and class II . The HLA test sera marketed, usually monoclonal antibodies are available in the market but at a very high cost. In contrast, HLA antibodies detected both in serum of multiparous women, polyclonal antibodies, are excellent reagents for HLA typing with a reasonable cost. The aim of our study was to screen HLA alloantibodies in multiparous and to identify exploitable antibodies as laboratory reagents, to the establishment of an HLA unit in the Department of Immunology of Cocody University Hospital at Abidjan.
2. Materials and Methods
One hundred twenty one women (121) in apparent good health, transfused or no-transfused were recruited at the obstetrics and Gynecology Department of Cocody University Hospital at Abidjan from January to June 2012. Their age ranged from 18 to 70 years. All participants had least 2 parities. Primiparous women, even with a known history of abortion were excluded from the study.
The reagents were consisted of 2 panels of 20 different cells (lymphocytes) each, from Bordeaux French Blood Agency including one panel for class I and one for Class II. A platelet pool "ripened" was also provided by Bordeaux French Blood Agency. Other reagents were used, including trypan blue 3 ‰, Hanks liquid (Seromed), plamagel (Rhone Poulenc), paraffin oil, liquid nitrogen, dithiothreitol (DTT) 0.01 mmol/L (Sigma), saturated cystine 0.02 mmol/L (Sigma), PBS buffer (Seromed).
The platform was consisted of plates Teresaki (Lab Nunc), a vending machine (self-DATTER® SERADOT CELL), an inverted microscope (Diavert-LEITZ®), a flow cytometer (Cytotron Absolute®).
Patients were selected after informed consent. Peripheral blood was collected from them by venipuncture in sterile dry tubes. Screening and identification tests for antibodies were performed on sera obtained after centrifugation and decantation of the blood.
A first step was to screen anti-HLA class I and class II by microlymphocytotoxicity method based on the lysis of lymphocytes panel by specific HLA antibodies contained in the serum in presence of rabbit complement. Then the revelation was made from an inverted microscope by observing the dye (trypan blue) within lysed cells.
Then in sera, class I antibodies were removed by absorption on a ripened pooled platelets (rich in class I antigens).
A second stage was to identify antibodies class by 3 methods:
-Treatment of positive sera by the DTT (Dithiotreitol) which inactivates IgM antibody;
-Heat effect (The reaction was negative beyond 22°C if antibody was IgM. If it was IgG, the reaction was positive regardless of the temperature: 4°C at 37°C);
-Flow cytometry with the labelling cells expressing HLA specificities by polyclonal HLA antibodies contained in the serum and its visualization by anti-IgG monoclonal antibodies or anti-IgM coupled to phycoerythrin.
Data processing and analysis were obtained by EPI-INFO V5.0, SPSS-PC. We used the parametric tests (Student's test) when the data distribution was normal. Otherwise, non-parametric tests (Mann-Vithney-Wilcoxon) were preferred.
Correlation coefficients (r2) were obtained using the software EPI-INFO V5.0, SPSS-PC. r2 evaluated strength of the relation between the anti-HLA antibody produced in immunized women and its antigenic specificity. The relation was low if r2 was ranged in [0-0.25]; average, in [0.25-0.5]; strong, in [0.5-0.75]; and very strong, in [0.75-0.1].
45 multiparous women (37.19%) had been HLA immunized. Class II antibodies were predominant.
|N (%)||13 (10.74%)||18 (14.88%)||14 (11.57%)||76 (62.81%)|
|N (%)||21 (77.78%)||5 (18.52%)||1 (3.7%)|
Specificity of HLA antibodies was identified at 17.78%. HLA-B7 specificity (Class I) was 37.5% and class II specificity (HLA-DR4, DR7, DR13, DR13+14, DRw52) was 62.5%. No anti-HLA-A specificity was found. Correlation coefficients (r2) for class I specificity (HLA-B7) were ranged from 0.79 to 1; while for class II specificities, r2 were ranged from 0.54 to 0.9.
|I||HLA-B7||3||0.79 to 1|
The HLA system is known to be the most polymorphic in humans . The distribution and frequency of HLA antigens vary greatly among different ethnic groups and this diversity has been postulated to evolve under unique selective pressure in different geographical areas . The complement-mediated microlymphocytotoxicity technique has been used as the standard for serologic typing of HLA class I and class II antigens . HLA typing sera are mainly obtained from multiparous alloimmunized women, and their HLA specificities are determined against a panel of lymphocytes with known HLA types. In mothers, several studies confirm the production of antibodies against paternal HLA antigens expressed by fetal cells because of their passage into the maternal circulation during pregnancy [9,10]. Production of HLA antibodies in the mother follows the dynamics of allogenic immune response. Paternal HLA molecules expressed by fetal cells that pass through the maternal bloodstream induce blast transformation of no histocompatible CD4+ which produce among other cytokines, IL-4 and IL-5 that stimulate production of antibodies by B lymphocytes and plasma cell progeny . Our study revealed a fetal-maternal HLA alloimmunization frequency at 37.19%. In a previous study on Ivorian women, an author had reported a lower rate of HLA immunization at 18.6% . This difference could be explained by the evolution of knowledge on the HLA system and especially the most effective techniques currently used for serological typing. Most of the data of HLA sensitization in pregnancy were obtained by use of a complement-dependent cytotoxicity assay. In many cases, antibodies cannot be detected by complement-dependent cytotoxicity as their level fades in time . Due to variation in immunization, a wide variation in the incidence of anti-HLA antibodies in the sera of pregnant women variation was ranged from 18% to 30% . Detection of HLA antibodies by the Luminex screening test revealed higher frequencies. With Luminex, anti-HLA immunization was observed beyond 50% [13,14]. The rate of HLA alloantibodies is increased with the number of pregnancies. The frequencies of lymphocytotoxic antibodies, HLA-ABC antibodies and HLA-DR antibodies, were studied in 66 women at delivery. They were, respectively, 18.2% and 9% in the first pregnancies, 27.3% and 4.5% in the second pregnancies, 50% and 27.3% in the multigravidous women (third pregnancy and more) . Immunization frequency increased with the number of children, reaching 74% in women with >2 deliveries .
Analysis of the results depending on the HLA class showed that HLA class II antibodies were predominant. This predominance of HLA class II antibodies could be explained by the important influence of class II antigens on B cells activation therefore the allogenic antibody response through cooperation TCD4+ and B lymphocytes. Rather the capacity of class I molecules to induce allogenic antibody response is low . The antibodies produced were predominantly IgG isotype. Some women had produced alloantibodies both IgM class and IgG class. These results were consistent with those reported in the literature [17,18]. HLA antibodies were usually IgG and rarely IgM . Studies have been reported that normal pregnant women develop anti-HLA antibodies, mostly after 20–28 weeks of gestation . Whether antibodies were of class I or class II, IgM or IgG isotype, HLA antibodies induced in vitro cytolysis. Detailed analysis of specificity of HLA antibodies in our study revealed only one specificity class I while 5 specificities class II. No specific HLA-A antiboby was identified in our study. Indeed, the predominance of sensitization in the HLA-B locus might be related to its larger polymorphism compared to the other HLA loci [20,21]. This negative result could be explained by the sample size. Also the frequency of HLA class I alleles and their linkage disequilibrium patterns differ significantly among human populations.
Study of the relationship between HLA class I antibodies and antigenic specificity reported correlation coefficients which were closed to 1. These good correlation coefficients showed that it was possible to constitute anti-HLA test sera from good maternal sera for local original typing tray.
There was an anti-HLA alloimmunization in the population of women multiparous in Abidjan. HLA antibodies produced were predominantly class II specificities, IgG isotype and great specificities to HLA antigens. These antibodies could therefore serve as reagents for HLA typing in our future HLA unit of the Department of Immunology at Abidjan pending production of monoclonal anti-HLA antibodies. But first, studies of a larger sample both of Africans and particular of Ivorians were needful to establish panels including all African specificities.
We would like to thank Department of Cellular Immunology of Bordeaux French Blood Agency (France) for their technical assistance in realization of this study.