CD4+ helper T cells mediate resistance to tuberculosis, presumably by
enhancing the antimicrobial activity of macrophages within which the M
ycobacterium tuberculosis organism grows. A first step in resistance s
hould be the presentation of mycobacterial antigens by macrophages to
CD4+ T cells. However, when the antigenic stimulus is limited to organ
isms growing in human monocytes, the organisms become sequestered from
immune CD4+ T cells. This block in presentation is selective for grow
ing mycobacteria and not for other stimuli. Sequestration would allow
replicating organisms to persist in infected individuals and may contr
ibute to virulence.