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Infection and Immunity, August 2006, p. 4954-4959, Vol. 74, No. 8
0019-9567/06/$08.00+0 doi:10.1128/IAI.01781-05
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Su-Hyung Park,1
Hye-Ju Kim,1
Seung-Chul Kim,2
Hyang-Ju Kang,1
Eun-Gae Lee,2
Soon-Geon Kwon,2
Byong-Moon Kim,3
Sung-Hee Lee,3
Won-Bae Kim,3
Young-Chul Sung,1*,
and
Sang-Nae Cho2,4*,
Division of Molecular and Life Sciences, Postech Biotech Center, Pohang University of Science & Technology, San 31 Hyoja-dong, Pohang 790-784, Korea,1 Department of Microbiology and Brain Korea 21 Project for Medical Sciences, Yonsei University College of Medicine, 134 Shinchon-dong, Seoul 120-752, Korea,2 Research Laboratories, Dong-A Pham. Co., Ltd., Yongin-si, Kyunggi-do 449-900, Korea,3 The International Vaccine Institute, Seoul 151-600, Korea4
Received 3 November 2005/ Returned for modification 20 December 2005/ Accepted 19 May 2006
Tuberculosis subunit vaccines codelivered with interleukin-12 (IL-12)-encapsulated microspheres (IL-12EM) are designed for a sustained release of IL-12 and could induce strong Th1 immune responses specific to Ag85A and ESAT-6. The adjuvant combination of IL-12EM plus AS01B was a more efficient way to induce a sustained Th1 immunity and protection against Mycobacterium tuberculosis.
Supplemental material for this article may be found at http://iai.asm.org/.
Present address: Emory Vaccine Center and Department of Microbiology and Immunology, Emory University School of Medicine, 1510 Clifton Road, Room G211, Atlanta, GA 30322.
Y.-C.S. and S.-N.C. contributed equally to this work.
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