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. 1999 Jun;154(6):1793–1804. doi: 10.1016/S0002-9440(10)65435-1

Table 8.

High Serum Anti-PGL-I Antibody Titer and in Situ Detection of PGL-I and Viable Ml. Bacilli in Skin Biopsy Specimen of Untreated Leprosy Patients and in Those in the Course of the Disease

Untreated patients Follow-up
Classification Patient number BI αPGL-I* PGL-I Ml. RNA Treatment status BI αPGL-I* PGL-I Ml. RNA
TT CPB05 0 + RFT 0
TT R90-36 0 ND + ND
BT R91-18 0 + RFT 0
BT R92-24 0 RFT 0
BT R92-11 0 ND
BT R87-60 0 + + ++ ND
BT R88-14 0 + + ND
BL R91-19 4+ + + +++ ND
BB R92-33 4+ + +++ On treatment (1 year) 1+ + +
BL R90-18 ND ND ND ND RFT 0 + +
BL R88-4 4+ + + +++ RFT 0
BL R89-81 4+ + +++ RFT 1+ +
BL R90-32 ND ND ND ND RFT 0 + + +§
BL R89-121 5+ + + RFT 0 + +
BL R90-21 4+ + + +++ RFT 0 + +
BL R88-1 ND ND ND ND RFT 1+ + + ++
RFT 0 + +

RFT, released from treatment; other abbreviations (TT, BT and BL) are as in Table 1 .

*Anti-PGL-I antibody titer in serum was measured by ELISA; serum values were considered high with OD >0.500.

PGL-I is detected by immunohistochemical analysis using MAb DZ-1.

Ml. RNA was detected by NASBA.

§Patient with poor compliance of therapy.

Patient was investigated for possible relapse.