Immunophenotypic characterisation of peripheral blood mononuclear cells in patients with MDR pulmonary tuberculosis
Hamdy Ali Mohammadien Mahmoud, Abeer M. Seinef, Ahmed Hassan Abdelaziz
Abstract
Hamdy Ali Mohammadien Mahmoud, Abeer M. Seinef, Ahmed Hassan Abdelaziz
Abstract
Objective: To determine the changes that take place in the sub populations of peripheral blood mononuclear cells of patients with MDR- tuberculosis and to compare their immune profile to responders to anti- tuberculosis drugs and healthy controls. Materials and Methods: Flow cytometry was used to determine the absolute numbers and percentages of T CD3, T CD4, T CD8, T CD19, T CD14, T CD25 and T CD56 cells in 25 patients with active pulmonary TB responding to treatment,15 MDR TB and in 20 healthy volunteers. Result: There were significant differences in the values of CD3, CD4, CD19, and CD56 T cells among the groups. CD4 was significantly higher in controls than Responders (39.5 ± 5.6 vs 33.5 ± 6,P < 0.002), and lower in Responders than MDR but not significant (33.5 ± 6 vs 38.1 ± 4.1,P < 0.06). CD3 was significantly lower in MDR than Responders and controls (45.12± 6.6 vs 52.± 11.4&66.2± 5.7, P < 0.0001). CD19 significantly higher in Responders than MDR and Controls (P < 0.04 & 0.03), lower in MDR than Controls but not significant (5.72± 1.7 vs 6.61± 4.2, p<0.8). CD56 significantly higher in MDR and Responders than Controls (P < 0.007 & 0.02), also higher in MDR than Responders but not significant (14.7±8.1 vs 9.60± 6.2, p<0.07). There were no significantly differences in the values of CD4 CD8, CD4 CD25, CD8, CD8 HLA and CD14 between all groups. Conclusion: There are significant changes in the cellular immune response particularly affecting the CD3, CD4, CD19 and CD56 T cells in MDR pulmonary TB. Therefore, further studies of these changes may have important implications on the development of diagnostic tools and treatment modalities.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective: To determine the changes that take place in the sub populations of peripheral blood mononuclear cells of patients with MDR- tuberculosis and to compare their immune profile to responders to anti- tuberculosis drugs and healthy controls. Materials and Methods: Flow cytometry was used to determine the absolute numbers and percentages of T CD3, T CD4, T CD8, T CD19, T CD14, T CD25 and T CD56 cells in 25 patients with active pulmonary TB responding to treatment,15 MDR TB and in 20 healthy volunteers. Result: There were significant differences in the values of CD3, CD4, CD19, and CD56 T cells among the groups. CD4 was significantly higher in controls than Responders (39.5 ± 5.6 vs 33.5 ± 6,P < 0.002), and lower in Responders than MDR but not significant (33.5 ± 6 vs 38.1 ± 4.1,P < 0.06). CD3 was significantly lower in MDR than Responders and controls (45.12± 6.6 vs 52.± 11.4&66.2± 5.7, P < 0.0001). CD19 significantly higher in Responders than MDR and Controls (P < 0.04 & 0.03), lower in MDR than Controls but not significant (5.72± 1.7 vs 6.61± 4.2, p<0.8). CD56 significantly higher in MDR and Responders than Controls (P < 0.007 & 0.02), also higher in MDR than Responders but not significant (14.7±8.1 vs 9.60± 6.2, p<0.07). There were no significantly differences in the values of CD4 CD8, CD4 CD25, CD8, CD8 HLA and CD14 between all groups. Conclusion: There are significant changes in the cellular immune response particularly affecting the CD3, CD4, CD19 and CD56 T cells in MDR pulmonary TB. Therefore, further studies of these changes may have important implications on the development of diagnostic tools and treatment modalities.
Key concepts: Medicine, CD19, Peripheral blood mononuclear cell, Internal medicine, CD8, Gastroenterology, CD3, Flow cytometry