Interferon‐γ responses after isoniazid chemotherapy for latent tuberculosis

Respirology - Tập 13 Số 3 - Trang 468-472 - 2008
Kazue Higuchi1, Nobuyuki Harada2, Toru Mori3
1Research Institute of Tuberculosis, Japan Anti-Tuberculosis Association, Tokyo, Japan
2Research Institute of Tuberculosis, Japan Anti‐Tuberculosis Association, and
3Leprosy Research Center, National Institute of Infectious Diseases, Tokyo, Japan

Tóm tắt

Background and objective:  Chemotherapy for Mycobacterium tuberculosis infection may decrease interferon (IFN)‐γ responses to early secretory antigenic target 6 and culture filtrate protein (CFP)‐10; a reaction that could be useful to monitor the success of treatment. We investigated IFN‐γ responses in subjects with latent TB infection before and after isoniazid (INH) chemotherapy.Methods:  A total of 48 patients who had contact with a TB patient in a psychiatric hospital were suspected to have latent TB infection on the basis of a positive QuantiFERON‐TB Gold (QFT‐G) test and were offered INH treatment for 6 months. After INH chemotherapy, IFN‐γ responses were again quantified and compared with initial measurements.Results:  Thirty‐four patients completed 6 months of therapy and 28 were retested. Seven (25%) had a negative test and the other patients showed an overall decline. Geometric mean for early secretory antigenic target 6 decreased from 1.398 to 0.362 (P < 0.001), and that for CFP‐10 from 0.312 to 0.120 (P < 0.001). A subsequent QFT‐G test carried out 18 months after chemotherapy showed no further decline of IFN‐γ responses.Conclusions:  If the success of chemotherapy is defined as negative conversion in the QFT‐G test, these results suggest that although the waning of QFT‐G responses as a result of chemotherapy is an important characteristic of IFN‐γ responses, the extent of waning would not be sufficient to allow effective monitoring of the success of chemotherapy because a majority of contacts still showed positive responses in the QFT‐G test even after chemotherapy.

Từ khóa


Tài liệu tham khảo

10.1016/S0140-6736(00)02742-2

10.1164/rccm.200402-179OC

Harada N, 2004, Usefulness of a novel diagnostic method of tuberculosis infection, QuantiFERON®TB‐2G, in an outbreak of tuberculosis, Kekkaku, 79, 637

10.1164/rccm.200402-232OC

10.1001/jama.293.22.2756

Funayama K, 2005, Usefulness of QuantiFERON®TB‐2G in contact investigation of a tuberculosis outbreak in a University, Kekkaku, 80, 527

Miyashita H, 2005, Detection of tuberculosis infection using a whole blood interferon gamma assay in a contact investigation–Evaluation using QuantiFERON®TB‐2G, Kekkaku, 80, 557

10.1086/504358

10.1186/1465-9921-7-77

10.4049/jimmunol.167.9.5217

10.1086/381754

10.1086/429245

10.1186/1471-2334-6-66

10.1086/499311

10.1186/1745-6673-1-7

10.1164/rccm.200511-1783OC

10.1164/rccm.200608-1109OC

10.1186/1465-9921-8-5

Maeda M, 1960, Further studies on the potency of purified protein derivatives of tuberculin (PPD‐s). 1st Report. Comparison of the potency of three preparations of PPD, Kekkaku, 35, 563

Kimura M, 2005, Comparison of erythema and induration as results of tuberculin tests, Int. J. Tuberc. Lung Dis., 9, 853

Ministry of Health, Labour and Welfare., 2004, Tuberculosis treatment standards (in Japanese), Ministry of Health, Labour and Welfare Bull, 238

10.1097/01.mcp.0000158726.13159.5e

10.1016/j.molmed.2007.03.004