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. 2001 Feb;102(2):146–156. doi: 10.1046/j.1365-2567.2001.01164.x

Table 1.

Effect of mycobacterial infection on human leucocyte antigen (HLA) expression by U937 cells

Percentage (± SD) of cells expressing surface antigen MFI (± SD) of cells expressing surface antigen


HLA Treatment Isotypic Ab* Specific Ab Isotypic Ab Specific Ab
HLA class II Uninfected 2·0 (± 1·0) 3·2 (± 2·6) 34·4 (± 20·9) 30·3 (± 18·1)
BCG infected 2·1 (± 0·6) 2·5 (± 1·3) 27·5 (± 11·2) 29·7 (± 15·9)
M. tb infected 2·0 (± 0·7) 2·2 (± 1·2) 35·0 (± 10·7) 32·8 (± 9·4)
HLA class I Uninfected 2·1 (± 1·9) 96·6 (± 2·6) 12·6 (± 13·4) 27·0 (± 12·1)
BCG infected 2·5 (± 1·7) 96·7 (± 2·1) 18·2 (± 19·5) 28·2 (± 8·9)
M. tb infected 2·3 (± 0·4) 94·3 (± 1·3) 23·8 (± 3·5) 59·5 (± 9·7)

These results are presented as the mean percentage (± SD) or mean fluorescence intensity (MFI) (± SD) of phorbol 12-myristate 13-acetate (PMA)-differentiated U937 cells expressing cell surface HLA class I or class II.

*

Isotypic controls were used in all cases to set cursors to allow 2% false positives. Ab, antibody.

HLA class I expression was significantly up-regulated (P < 0·05) following infection with Mycobacterium tuberculosis (M. tb) H37Rv but not with bacillus Calmette–Guérin (BCG).