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Updated: Jun 5, 2026
Protective Efficacy and Pulmonary Immune Response Following Subcutaneous and Intranasal BCG Administration in Mice
Published on: September 19, 2016
[Correlation between the expression of perforin in T-lymphocyte subsets and antituberculosis in mice vaccinated with
Jian-Ping Lei1, Yin Wan, Jun Zhou
1Chest Hospital of Jiangxi Province, Nanchang 330006, China.
Objective:
To investigate the relationship between the expression of perforin in T-lymphocyte subsets and antituberculosis in mice vaccinated with bacillus calmette-guerin (BCG).
Methods:
120 KM male mice were divided into a Control group (group C, n = 40, 20 each in group C1 or C2), a BCG vaccinated group (group B, n = 40, 20 each in group B1 or B2), a Tuberculosis group (TB group, n = 20), and a BT group, in which the mice were attacked by Mycobacterium tuberculosis H(37)Rv (MTB) after acquired immunity by vaccination with BCG (n = 20). Initially, mice in group B1, B2 and BT were vaccinated with BCG synchronously. Three month later, mice in group BT and TB were attacked by MTB synchronously. Samples of blood, lung, liver and spleen of mice in group C1 and B1 were collected at the same time. One month later again, Samples of blood, lung, liver and spleen of mice in group C2, B2, BT and TB were collected at the same time. Samples of blood were assayed for T-lymphocyte subsets expressing perforin (PFN(+)). The positive numbers of PFN(+) [CD(3)(+), CD(4)(+), CD(8)(+), CD(4)(+)CD(8)(+) double positive (CD(4)(+)CD(8)(+))] T lymphocytes and their percentages were assayed by flow cytometer. Specimens of lung, liver and spleen were examined for pathology and bacteriology.
Results:
All the mice in the TB group acquired tuberculosis and the mortality was 55% (11/20) within 1 month. There were no tuberculosis and no death in mice of C, B and BT groups during the observation period. The amount of PFN(+) CD(8)(+) T lymphocytes in B group [(5.9 ± 0.9) × 10(3)] was significantly higher than that in C group [(4.8 ± 0.8) × 10(3)] (F = 42.24, P < 0.01). The PFN(+) CD(8)(+)% in TB group [(5.6 ± 0.9)%] was significantly less than that in B group [(7.3 ± 1.1)%] (F = 35.51, P < 0.05). For Mice in the BT group, the amount of PFN(+) (CD(3)(+), CD(8)(+), CD(4)(+)CD(8)(+)) T lymphocytes [(20.1 ± 5.5) × 10(3), (8.7 ± 0.4) × 10(3), 72 ± 19] and their CD(3)(+)%, CD(8)(+)%, CD(4)(+)CD(8)(+)% [(23.3 ± 3.3)%, (10.7 ± 1.6)%, (0.084 ± 0.015)%] were all higher than those in the B group [(13.0 ± 3.2) × 10(3), (5.9 ± 0.9) × 10(3), 36 ± 5, (15.5 ± 1.7)%, (7.3 ± 1.1)%, (0.044 ± 0.007)%] or the C group [(11.1 ± 3.0) × 10(3), (4.8 ± 0.8) × 10(3), 30 ± 7, (14.9 ± 1.7)%, (6.7 ± 0.9)%, (0.040 ± 0.006)%] or the TB group [(12.6 ± 1.6) × 10(3), (5.0 ± 0.1) × 10(3), 31 ± 3, (14.0 ± 1.7)%, (5.6 ± 0.9)%, (0.035 ± 0.005)%] (F = 14.23 - 74.98, P < 0.01 or P < 0.05), and the CD(4)(+)/CD(8)(+) in BT group (0.54 ± 0.17) was significantly lower than that in C group (0.76 ± 0.22) (F = 4.54, P < 0.01).
Conclusions:
Pre-vaccination with BCG increased PFN(+) CD(8)(+) T lymphocytes in the host. Acquired immunity by BCG vaccination can protect the host from attack by Mycobacterium tuberculosis. Increased PFN(+) (CD(3)(+), CD(8)(+), CD(4)(+)CD(8)(+)) T lymphocytes may be involved. The expression level of PFN by T lymphocytes may be an important marker for antituberculosis immunity.
