Humoral immunity and haemoglobin F (HbF) status in steady state adult Nigerian sickle cell disease patients with asymptomatic malaria

2Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.

Abstract

Aim: Nigeria, where malaria is prevalent, has the largest sickle cell gene pool in the world. To this end, there is a need for increased understanding of the pathophysiology of HbSS patients in a malaria endemic zone to reduce mortality. Haematology Department, University College Hospital, Ibadan, Nigeria. Materials and methods: The levels of HbF, IgG, IgA, IgM, transferin (TRF), C-reactive protein (CRP), and haptoglobin (HPT) were determined in 14 Nigerians having HbAA genotype with malaria parasitaemia (HbAA +MP), 17 Nigerians having haemoglobin AA genotype without malaria parasitaemia (HbAA -MP), 15 Nigerians having haemoglobin SS genotype without malaria parasitaemia (HbSS -MP), and 14 Nigerians having HbSS with malaria parasitaemia (HbSS +MP). Results: The levels of Ig classes were statistically similar in all the groups. CRP was significantly increased in HbSS -MP compared with HbAA +MP or HbAA -MP. The levels of TRF and HPT were significantly reduced in HbSS -MP or HbSS +MP compared with HbAA -MP. Also TRF and HPT were significantly reduced in HbSS +MP compared with HbSS -MP. Conclusion: These observations may be related to RBC haemolysis especially in HbSS +MP. © TÜBİTAK.

Cite

CITATION STYLE

APA

Olaniyi, J. A., & Arinola, G. O. (2009). Humoral immunity and haemoglobin F (HbF) status in steady state adult Nigerian sickle cell disease patients with asymptomatic malaria. Turkish Journal of Medical Sciences, 39(6), 953–957. https://doi.org/10.3906/sag-0901-8

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free