2011 Fiscal Year Final Research Report
Subunit vaccine for Tbc with mucosal adjuvant activity of LT
| Project/Area Number |
21590497
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Bacteriology (including Mycology)
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| Research Institution | Fujita Health University |
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Principal Investigator |
TSUJI Takao 藤田保健衛生大学, 医学部, 教授 (60171998)
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| Project Period (FY) |
2009 – 2011
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| Keywords | 結核抗原 / 毒素原性大腸菌 / 下痢毒素(LT) / Ag85A, B, C / CFP-10 |
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| Research Abstract |
Ag85A, B or C of BCG and CFP-10, EAST-6, PPE or TB7.3 of Tbc were overproduced and purified. Although TB7.3 was aggregated and could not be purified, the others were purified and used for antigens to immunize mice with mutant LT as the mucosal adjuvant. We determined that the mice immunized with Ag85A, B or C plus mLT were not effective for prevention of BCG or Tbc infection. As we need much time to determine whether CFP-10, EAST-6, PP E or TB7.3 from Tbc will be effective to Tbc infection as the vaccine, we are doing some experiments to determine it.
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[Journal Article] Randomized placebo-controlled clinical trial of immunoglobulin Y as adjunct to standard supportive therapy for rotavirus-associated diarrhea among pediatric patients.2012
Author(s)
Rahman S, Higo-Moriguchi K, Htun KW, Taniguchi K, Icatlo FC Jr, Tsuji T, Kodama Y, Van Nguyen S, Umeda K, Oo HN, Myint YY, Htut T, Myint SS, Thura K, Thu HM, Fatmawati NN, Oguma K.
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Journal Title
Vaccine
Volume: (in press)
Peer Reviewed
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