Evidence map›Paper›PMID 40397034›Full record

ArticleMolecular biology reports2025

The MNS blood group system in Tunisian blood donors: common and rare alleles.

Mohamed Hichem Sellami, Eya Ghazouani, Sondess Hadj Fredj, Hamida Ferchichi, Manel Chaabane, Houda Kaabi, Taieb Messaoud, Slama Hmida

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Mohamed Hichem Sellami"Immunogenetics, Cell Therapy and Blood Transfusion" Research Laboratory (LR20SP05), Department of Immunohaematology, National Blood Transfusion Centre of Tunis, University of Tunis El Manar, 13 Street of Djbel Lakhdar, Bab Saadoun, Tunis, 1006, Tunisia. mohamedhichem.sellami@rns.tn.ORCID https://orcid.org/0000-0002-0527-8760
Eya Ghazouani"Immunogenetics, Cell Therapy and Blood Transfusion" Research Laboratory (LR20SP05), Department of Immunohaematology, National Blood Transfusion Centre of Tunis, University of Tunis El Manar, 13 Street of Djbel Lakhdar, Bab Saadoun, Tunis, 1006, Tunisia.
Sondess Hadj FredjBiochemistry Laboratory, Bechir Hamza Children's Hospital, Bab Saadoun, Tunis, 1007, Tunisia.
Hamida Ferchichi"Immunogenetics, Cell Therapy and Blood Transfusion" Research Laboratory (LR20SP05), Department of Immunohaematology, National Blood Transfusion Centre of Tunis, University of Tunis El Manar, 13 Street of Djbel Lakhdar, Bab Saadoun, Tunis, 1006, Tunisia.
Manel Chaabane"Immunogenetics, Cell Therapy and Blood Transfusion" Research Laboratory (LR20SP05), Department of Immunohaematology, National Blood Transfusion Centre of Tunis, University of Tunis El Manar, 13 Street of Djbel Lakhdar, Bab Saadoun, Tunis, 1006, Tunisia.
Houda Kaabi"Immunogenetics, Cell Therapy and Blood Transfusion" Research Laboratory (LR20SP05), Department of Immunohaematology, National Blood Transfusion Centre of Tunis, University of Tunis El Manar, 13 Street of Djbel Lakhdar, Bab Saadoun, Tunis, 1006, Tunisia.
Taieb MessaoudBiochemistry Laboratory, Bechir Hamza Children's Hospital, Bab Saadoun, Tunis, 1007, Tunisia.
Slama Hmida"Immunogenetics, Cell Therapy and Blood Transfusion" Research Laboratory (LR20SP05), Department of Immunohaematology, National Blood Transfusion Centre of Tunis, University of Tunis El Manar, 13 Street of Djbel Lakhdar, Bab Saadoun, Tunis, 1006, Tunisia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe MNS blood group system is highly complex and characterized by the presence of major polymorphic antigens, namely MNS1/MNS2 and MNS3/MNS4. This study aims to examine the genetic basis of the common MNS antigens in Tunisian blood donors and discussed their importance in transfusion immunology. METHODS AND

resultsA group of 229 Tunisian blood donors were genotyped for the major alleles GYPA*01, GYPA*02, GYPB*03 and GYPB*04 using the SSP-PCR method. A specific GYPA region was sequenced in some subjects to examine if there is a rare allele. The statistical analysis was done using the HaploView Software. The molecular analysis showed that 4 blood donors are probably carrier of a rare GYPA allele. Furthermore, it appeared that the GYPA*01 and GYPB*04 alleles; and the GYPA*01-GYPB*04 haplotype are predominant in this series. As for the phenotype, the study showed that the MNS:1,2,-3,4 type is the most frequent in recruited blood donors.

conclusionsOverall, the study showed a balanced distribution of the targeted alleles. Furthermore, the observed frequencies appeared to be in harmony with that reported in other populations. Considering the importance of these findings, we think that this work will be an important contribution to the field of public health and epidemiology.

Indexed as

Blood DonorsGlycophorinsMNSs Blood-Group SystemAdultAllelesBlood Group AntigensFemaleGene FrequencyGenotypeHaplotypesHumansMaleTunisiaBlood Group AntigensGlycophorinsGYPA protein, humanGYPB protein, humanMNSs Blood-Group SystemAlloimmunizationBloodMNS antigensPCR-SSPTunisians

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.