G. Plum et al., SERUM ANTIBODY REACTIVITY TO RECOMBINANT MIG AND WHOLE-CELL ANTIGENS IN MYCOBACTERIUM-AVIUM INFECTION, Zentralblatt fur Bakteriologie, 284(2-3), 1996, pp. 348-360
Mycobacterium avium is a significant opportunistic pathogen in immunoc
ompromised patients. Moreover, the prevalence of infections in patient
s without known predisposing conditions has also been increasing in re
cent years. Patients would greatly benefit from early diagnosis of dis
seminated infection. Serodiagnostic tests have already been promising
in tuberculosis and immunocompetent patients but studies in HIV-infect
ed patients and humoral response to M. avium antigens resulted in conf
licting data. We have evaluated the use of the phagocytosis-induced MI
G protein of M. avium as a diagnostic antigen. Serum antibody levels o
f M. avium-infected, HN-negative patients were significantly elevated
for the recombinant of MIG (p < 0.001) and also for M. avium whole-cel
l antigens (p < 0.025) as compared to controls. In contrast, HIV-infec
ted patients with disseminated M. avium infection demonstrated also el
evated levels of antibody for the whole-cell antigen (p < 0.00001) but
a decreased reactivity for the MIG antigen (p < 0.007). The recombina
nt antigen proved to have no cross-reactivity with M. tuberculosis ant
igens as antibody levels were decreased in tuberculosis patients Ip <
0.001). Therefore, a simultaneous serological test using recombinant M
IG and the whole cell antigens might be helpful in the sometimes probl
ematic diagnosis of M. avium infections in patients without predisposi
ng conditions.