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<title>PHAGOCYTIC MECHANISM AND ITS PLASMA MODULATORS IN  PULMONARY TUBERCULOSIS PATIENTS ON ANTI-TUBERCULOSIS  CHEMOTHERAPY AND ZINC SUPPLEMENT B</title>
<link href="http://hdl.handle.net/123456789/690" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/123456789/690</id>
<updated>2026-04-20T05:57:08Z</updated>
<dc:date>2026-04-20T05:57:08Z</dc:date>
<entry>
<title>PHAGOCYTIC MECHANISM AND ITS PLASMA MODULATORS IN  PULMONARY TUBERCULOSIS PATIENTS ON ANTI-TUBERCULOSIS  CHEMOTHERAPY AND ZINC SUPPLEMENT B</title>
<link href="http://hdl.handle.net/123456789/691" rel="alternate"/>
<author>
<name>EDEM, VICTORY FABIAN</name>
</author>
<id>http://hdl.handle.net/123456789/691</id>
<updated>2022-01-21T14:56:58Z</updated>
<published>2019-07-01T00:00:00Z</published>
<summary type="text">PHAGOCYTIC MECHANISM AND ITS PLASMA MODULATORS IN  PULMONARY TUBERCULOSIS PATIENTS ON ANTI-TUBERCULOSIS  CHEMOTHERAPY AND ZINC SUPPLEMENT B
EDEM, VICTORY FABIAN
The progression of tuberculosis (TB) caused by Mycobacterium tuberculosis (M. tuberculosis) from &#13;
latent to drug-sensitive TB (DS-TB) or multi-drug resistant TB (MDR-TB) depends on factors &#13;
including host-pathogen interactions. The nature and course of these interactions are largely &#13;
determined by host zinc levels, a function of host immune responses. Clear understanding of these &#13;
interactions is crucial to identify protection mechanisms, which are not completely elucidated. This &#13;
study was designed to assess phagocytic mechanism and its plasma modulators in TB patients before &#13;
and during anti-TB chemotherapy with or without zinc supplementation.&#13;
Ethical approval (UI/EC/13/0340) was obtained and 160 consenting participants (50 MDR-TB&#13;
patients, 60 DS-TB patients and 50 controls) were enrolled. The MDR-TB and DS-TB patients were &#13;
treated with anti-tuberculosis chemotherapy. Thirty DS-TB patients received zinc supplement. Blood &#13;
sample was collected and plasma obtained from patients at baseline, 2, 4 and 6 months of anti-TB &#13;
chemotherapy with or without zinc supplement. Phagocytic mechanism [percentage leucocyte &#13;
migration (%LM) and intracellular killing (%NBT)] were determined by microscopy. Interleukin 6 &#13;
(IL-6) and 8 (IL-8) were determined using ELISA; superoxide dismutase (SOD), myeloperoxidase &#13;
(MPO), hydrogen peroxide (H2O2) and nitric oxide (NO) were determined by spectrophotometry. Iron &#13;
(Fe), zinc (Zn) and copper (Cu) were determined using AAS while vitamins A, C, D and E were &#13;
determined by HPLC. Data was analysed using Kruskal-Wallis, Mann-Whitney U, Friedman and&#13;
Wilcoxon signed rank tests at α0.05.&#13;
In MDR-TB patients, baseline levels of %LM (91.5±0.9 vs 55.0±2.2), IL-6, IL-8 (186.4±29.9 vs &#13;
3.7±0.8; 1116.4±198.3 vs 18.9±2.4 pg/mL) and vitamin C (4.80±0.2 vs 3.5±0.7 mg/dL) were &#13;
significantly higher while MPO (7.5±0.3 vs 8.3±0.3 U/mL), NO (9.2±0.8 vs 14.8±1.3 µmol/L), Fe, Zn &#13;
and Vitamin A (92.2±2.3 vs 123.3±1.2; 62.6±1.0 vs 118.3±3.1; 49.8±2.6 vs 80.8±6.4 µg/dL) were &#13;
lower compared with controls. In DS-TB patients, baseline IL-8 (162.6±56.3 vs 18.9±2.4 pg/mL) and &#13;
MPO (9.3±0.4 vs 8.3±0.3 U/mL) were significantly higher while SOD (0.2±0.0 vs 0.3±0.0 U/mL), &#13;
H2O2 (269.1±8.3 vs 313.8±7.4 µmol/L), NO (10.3±1.6 vs 14.8±1.3 µmol/L), Zn (81.3±6.3 vs &#13;
118.3±3.1 µg/dL), vitamins C and E (0.7±0.0 vs 3.5±0.7; 1.1±0.1 vs 1.7±0.3 mg/dL) were lower&#13;
compared with controls. At 2 months of anti-TB chemotherapy compared with baseline, MPO &#13;
(11.1±0.3 vs 9.6±0.3 U/mL) was significantly increased in DS-TB patients on anti-TB chemotherapy &#13;
alone while SOD (0.2±0.0 vs 0.1±0.0 U/mL), MPO (17.5±1.0 vs 9.0±0.7 U/mL) and NO (25.7±2.4 vs &#13;
20.7±1.8 µmol/L) were increased in DS-TB patients on chemotherapy and zinc supplement. At 4 &#13;
months of anti-TB chemotherapy, MPO (18.7±1.2 vs 9.0±0.7 U/mL) and NO (26.8±2.2 vs 20.7±1.8 &#13;
µmol/L) were significantly increased in DS-TB patients on anti-TB chemotherapy and zinc &#13;
supplement compared with baseline. At 6 months of anti-TB chemotherapy in DS-TB patients &#13;
compared with baseline, H2O2 and NO (372.9±6.1 vs 316.7±7.9; 14.7±1.4 vs 12.0±1.3 µmol/L) were &#13;
4&#13;
increased in patients on anti-TB chemotherapy alone while MPO (20.2±1.3 vs 9.0±0.7 U/mL) &#13;
increased in patients on anti-TB chemotherapy and zinc supplement.&#13;
Zinc supplementation with anti-tuberculosis chemotherapy improved phagocytic mechanism and its &#13;
plasma modulators in TB patients from 2 months of treatment
</summary>
<dc:date>2019-07-01T00:00:00Z</dc:date>
</entry>
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