The objective of this study was to catalogue clinically significant antigens of the Rh and Kell blood group systems among regular donors at the Regional Blood Transfusion Center (RBTC) of Bouaké. A total of 129 donors were included. ABO, Rh, and Kell typing were performed on samples collected from these donors using both slide and gel card methods. Among the donors, 120 (93.02%) were male and 9 (6.98%) female, aged between 19 and 58 years, with a mean age of 32.75 ± 7.9 years. The distribution of ABO phenotypes was as follows: O (49.6%, n = 64), A (17.1%, n = 22), B (27.1%, n = 35), and AB (6.2%, n = 8). Regarding the Rhesus (Rh) system, out of the 120 donors typed, 66 (51.2%) were RhD positive and 63 (48.8%) RhD negative. The most prevalent Rh antigens were c and e, each present in 99.2% of donors, followed by D (51.2%), C (17.1%), and E (10.3%). The observed Rh phenotypes were predominantly: ddccee (37.2%), Dccee (35.7%), ddCcee (11.6%), DccEe (8.5%), DCcee (4.6%), DccEE (1.6%), and DCCee (0.8%). The frequency of the Kell antigen (K) among these donors was 1.6%. The associated erythrocyte phenotypes were mainly O- cc dd ee K+ and O+ cc D Ee K+. The establishment of this erythrocyte phenotype database represents a valuable tool to enhance transfusion safety and reduce the risk of post-transfusion complications.
| Published in | International Journal of Immunology (Volume 14, Issue 1) |
| DOI | 10.11648/j.iji.20261401.12 |
| Page(s) | 10-16 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2026. Published by Science Publishing Group |
Phenotype, ABO, Rh, Kell, Blood Donor
Number of blood donations | Rh D- n (%) | Rh D+ n (%) | Total n (%) |
|---|---|---|---|
= 1 | 3 (2.33) | 12 (9.30) | 15 (11.63) |
[2-3] | 20 (15.5) | 27 (20.93) | 47 (36.43) |
[4-8] | 40 (31) | 27 (20.93) | 67 (51.94) |
Total | 63 (48.8) | 66 (51.2) | 129 (100) |
Age (Years) | Sex | Total n (%) | |
|---|---|---|---|
Male n (%) | Feminine n (%) | ||
[19-25] | 27 (20.93) | 4 (3.10) | 31 (24.03) |
[25-35] | 46 (35.66) | 2 (1.55) | 48 (37.21) |
[35-45] | 36 (27.91) | 1(0.77) | 37 (28.68) |
[45-55] | 10 (7.75) | 1(0.77) | 11 (8.53) |
[55-65] | 1 (0.77) | 1(0.77) | 2 (1.55) |
ABO RH | A | B | AB | O |
|---|---|---|---|---|
C | 1.6 | 4.7 | 1.6 | 9.3 |
c | 17.1 | 27.1 | 6.2 | 48.8 |
D | 7 | 17.1 | 3.9 | 23.3 |
E | 0.8 | 3.1 | 2.3 | 3.9 |
e | 17.1 | 26.4 | 5.4 | 49.6 |
CW | 0 | 0 | 0 | 0 |
K+ | 0 | 0 | 0 | 1.6 |
Phenotype | Frequency (%) |
|---|---|
DCCee | 0.8 |
DCcee | 4.6 |
Dccee | 35.7 |
DccEE | 1.6 |
DccEe | 8.5 |
ddCcee | 11.6 |
ddccee | 37.2 |
Phenotype | Blood groups | Total | |||
|---|---|---|---|---|---|
A n (%) | B n (%) | AB n (%) | O n (%) | ||
CC D ee K- | 0 | 0 | 0 | 1 (0.77) | 1 (0.77) |
Cc D ee K- | 0 | 3 (2.32) | 1 (0.77) | 2 (1.55) | 6 (4.65) |
cc D ee K- | 8 (6.20) | 15 (11.63) | 1 (0.77) | 22 (17.05) | 46 (35.66) |
cc D EE K- | 0 | 1 (0.77) | 1 (0.77) | 0 | 2 (1.55) |
cc D Ee K- | 1 (0.77) | 3 (2.32) | 2 (1.55) | 4 (3.10) | 10 (7.75) |
cc D Ee K+ | 0 | 0 | 0 | 1 (0.77) | 1 (0.77) |
cc dd ee K+ | 0 | 0 | 0 | 1 (0.77) | 1 (0.77) |
Cc dd ee K- | 2 (1.55) | 3 (2.32) | 1 (0.77) | 9 (6.98) | 15 (11.63) |
cc dd ee K- | 11 (8.53) | 10 (7.75) | 2 (1.55) | 24 (18.60) | 47 (36.43) |
Total | 22 (17.05) | 35 (27.13) | 8 (6.20) | 64 (49.61) | 129 (100) |
RBTC | Regional Blood Transfusion Center |
Rh | Rhesus |
HIV | Human Immunodeficiency Virus |
EDTA | Ethylenediaminetetraacetic Acid |
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APA Style
N’gou, M. E. R. E., Kouame, K. E., Nenelou, N. F., Siransy, L., Kabore, S., et al. (2026). Erythrocyte Phenotype Profiling in Repeat Blood Donors: A Cross-sectional Study in the Gbêkê Region, Côte d’Ivoire. International Journal of Immunology, 14(1), 10-16. https://doi.org/10.11648/j.iji.20261401.12
ACS Style
N’gou, M. E. R. E.; Kouame, K. E.; Nenelou, N. F.; Siransy, L.; Kabore, S., et al. Erythrocyte Phenotype Profiling in Repeat Blood Donors: A Cross-sectional Study in the Gbêkê Region, Côte d’Ivoire. Int. J. Immunol. 2026, 14(1), 10-16. doi: 10.11648/j.iji.20261401.12
@article{10.11648/j.iji.20261401.12,
author = {M’boh Epi Reine Elisabeth N’gou and Konan Eugène Kouame and Natacha Fleur Nenelou and Liliane Siransy and Saydou Kabore and Bamory Dembele and Mamadou Yassongui Sekongo},
title = {Erythrocyte Phenotype Profiling in Repeat Blood Donors:
A Cross-sectional Study in the Gbêkê Region, Côte d’Ivoire},
journal = {International Journal of Immunology},
volume = {14},
number = {1},
pages = {10-16},
doi = {10.11648/j.iji.20261401.12},
url = {https://doi.org/10.11648/j.iji.20261401.12},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.iji.20261401.12},
abstract = {The objective of this study was to catalogue clinically significant antigens of the Rh and Kell blood group systems among regular donors at the Regional Blood Transfusion Center (RBTC) of Bouaké. A total of 129 donors were included. ABO, Rh, and Kell typing were performed on samples collected from these donors using both slide and gel card methods. Among the donors, 120 (93.02%) were male and 9 (6.98%) female, aged between 19 and 58 years, with a mean age of 32.75 ± 7.9 years. The distribution of ABO phenotypes was as follows: O (49.6%, n = 64), A (17.1%, n = 22), B (27.1%, n = 35), and AB (6.2%, n = 8). Regarding the Rhesus (Rh) system, out of the 120 donors typed, 66 (51.2%) were RhD positive and 63 (48.8%) RhD negative. The most prevalent Rh antigens were c and e, each present in 99.2% of donors, followed by D (51.2%), C (17.1%), and E (10.3%). The observed Rh phenotypes were predominantly: ddccee (37.2%), Dccee (35.7%), ddCcee (11.6%), DccEe (8.5%), DCcee (4.6%), DccEE (1.6%), and DCCee (0.8%). The frequency of the Kell antigen (K) among these donors was 1.6%. The associated erythrocyte phenotypes were mainly O- cc dd ee K+ and O+ cc D Ee K+. The establishment of this erythrocyte phenotype database represents a valuable tool to enhance transfusion safety and reduce the risk of post-transfusion complications.},
year = {2026}
}
TY - JOUR T1 - Erythrocyte Phenotype Profiling in Repeat Blood Donors: A Cross-sectional Study in the Gbêkê Region, Côte d’Ivoire AU - M’boh Epi Reine Elisabeth N’gou AU - Konan Eugène Kouame AU - Natacha Fleur Nenelou AU - Liliane Siransy AU - Saydou Kabore AU - Bamory Dembele AU - Mamadou Yassongui Sekongo Y1 - 2026/02/26 PY - 2026 N1 - https://doi.org/10.11648/j.iji.20261401.12 DO - 10.11648/j.iji.20261401.12 T2 - International Journal of Immunology JF - International Journal of Immunology JO - International Journal of Immunology SP - 10 EP - 16 PB - Science Publishing Group SN - 2329-1753 UR - https://doi.org/10.11648/j.iji.20261401.12 AB - The objective of this study was to catalogue clinically significant antigens of the Rh and Kell blood group systems among regular donors at the Regional Blood Transfusion Center (RBTC) of Bouaké. A total of 129 donors were included. ABO, Rh, and Kell typing were performed on samples collected from these donors using both slide and gel card methods. Among the donors, 120 (93.02%) were male and 9 (6.98%) female, aged between 19 and 58 years, with a mean age of 32.75 ± 7.9 years. The distribution of ABO phenotypes was as follows: O (49.6%, n = 64), A (17.1%, n = 22), B (27.1%, n = 35), and AB (6.2%, n = 8). Regarding the Rhesus (Rh) system, out of the 120 donors typed, 66 (51.2%) were RhD positive and 63 (48.8%) RhD negative. The most prevalent Rh antigens were c and e, each present in 99.2% of donors, followed by D (51.2%), C (17.1%), and E (10.3%). The observed Rh phenotypes were predominantly: ddccee (37.2%), Dccee (35.7%), ddCcee (11.6%), DccEe (8.5%), DCcee (4.6%), DccEE (1.6%), and DCCee (0.8%). The frequency of the Kell antigen (K) among these donors was 1.6%. The associated erythrocyte phenotypes were mainly O- cc dd ee K+ and O+ cc D Ee K+. The establishment of this erythrocyte phenotype database represents a valuable tool to enhance transfusion safety and reduce the risk of post-transfusion complications. VL - 14 IS - 1 ER -