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Volumn 63, Issue 17, 1998, Pages 5983-5999

Synthesis of glycoconjugate vaccines against Shigella dysenteriae type 1

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOCONJUGATE; VACCINE;

EID: 0032555442     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo980660a     Document Type: Article
Times cited : (77)

References (90)
  • 7
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    • note
    • The commercial vaccines [Pneumovax 23, (MSD) and Pnu-Immune (Lederle-Praxis)] contain 25 μg of highly purified capsular polysaccharides of each of the 23 most invasive pneumococci.
  • 12
    • 0000308747 scopus 로고    scopus 로고
    • An exception is the CPS of Group A Neisseria meningitidis that induces protective antibody levels at all ages including infants: Robbins, J. B.; Schneerson, R.; Gotschlich, E. C. Lancet 1997, 350, 1709.
    • (1997) Lancet , vol.350 , pp. 1709
    • Robbins, J.B.1    Schneerson, R.2    Gotschlich, E.C.3
  • 22
    • 15644366769 scopus 로고    scopus 로고
    • note
    • Commercial conjugate vaccines against Haemophilus influenzae type b: ProHiBit (Connaught), HibTITER (Lederle-Praxis), PedvaxHIB (MSD), ActHIB (Merieux/Connaught).
  • 24
    • 0000195154 scopus 로고    scopus 로고
    • Levine, M. M., Woodrow, G. C., Kaper, J. B., Cobon, G. S., Eds.; Marcel Dekker
    • Klein, D. L.; Ellis, R. W. New Generation Vaccines; Levine, M. M., Woodrow, G. C., Kaper, J. B., Cobon, G. S., Eds.; Marcel Dekker: 1997; p 503.
    • (1997) New Generation Vaccines , pp. 503
    • Klein, D.L.1    Ellis, R.W.2
  • 27
    • 0001951250 scopus 로고    scopus 로고
    • Levine, M. M., Woodrow, G. C., Kaper, J. B., Cobon, G. S., Eds.; Marcel Dekker
    • Robbins, J. B.; Schneerson, R.; Szu, S. C. New Generation Vaccines; Levine, M. M., Woodrow, G. C., Kaper, J. B., Cobon, G. S., Eds.; Marcel Dekker: 1997; p 803.
    • (1997) New Generation Vaccines , pp. 803
    • Robbins, J.B.1    Schneerson, R.2    Szu, S.C.3
  • 29
    • 85025392991 scopus 로고
    • In an exceptional case, a protein conjugate of a disaccharide corresponding to only one repeating unit of type 3 pneumococcus provided protection in adult rabbits: Goebel, W. F. J. Exp. Med. 1940, 72, 33.
    • (1940) J. Exp. Med. , vol.72 , pp. 33
    • Goebel, W.F.1
  • 36
    • 0020182243 scopus 로고
    • Joint Commission on Biological Nomenclature
    • The term "oligosaccharide" is used to denote the saccharides synthesized in this work, while cognizant of the fact that by definition (Joint Commission on Biological Nomenclature, Eur. J. Biochem. 1982, 126, 433) oligosaccharides contain up to and including 10 monosaccharide units.
    • (1982) Eur. J. Biochem. , vol.126 , pp. 433
  • 52
    • 0002503127 scopus 로고    scopus 로고
    • Khan, S. H., O'Neill, R. A., Eds.; Harwood Academic Publishers
    • (b) Norberg, T. Modern methods in carbohydrate synthesis; Khan, S. H., O'Neill, R. A., Eds.; Harwood Academic Publishers: 1996; p 82.
    • (1996) Modern Methods in Carbohydrate Synthesis , pp. 82
    • Norberg, T.1
  • 63
    • 15644373651 scopus 로고    scopus 로고
    • note
    • In one unpublished approach, an eicosasaccharide was prepared by linear condensation of five repeating units that contained an azido function at C-2 of the glucose unit. Numerous attempts to convert the azido to acetamido groups in that protected saccharide proved to be abortive.
  • 76
  • 79
    • 0002218582 scopus 로고
    • Other approaches to ω-aldehydoalkyl glycosides include (a) ozonolysis of O-allyl glycosides (Bernstein, M. E.; Hall, L. D. Carbohydr. Res. 1980, 78, C1).
    • (1980) Carbohydr. Res. , vol.78
    • Bernstein, M.E.1    Hall, L.D.2
  • 80
    • 0027222044 scopus 로고
    • (b) Swern oxidation of ω-hydroxyalkyl glycosides (Pozsgay, V. Glycoconj. J. 1993, 10, 133).
    • (1993) Glycoconj. J. , vol.10 , pp. 133
    • Pozsgay, V.1
  • 82
    • 15644378068 scopus 로고    scopus 로고
    • note
    • (d) Use of a secondary spacer that features a protected aldehydo moiety (ref 53).
  • 86
    • 0031214782 scopus 로고    scopus 로고
    • Characterization of the saccharide-protein conjugates by MALDI-TOF mass spectrometry avoids the errors of the traditionally used colorimetric procedures for saccharide determination that may reach 50%: Dambra, A. J.; Baugher, J. E.; Concannon, P. E.; Pon, R. A.; Michon, F. Anal. Biochem. 1997, 250, 228.
    • (1997) Anal. Biochem. , vol.250 , pp. 228
    • Dambra, A.J.1    Baugher, J.E.2    Concannon, P.E.3    Pon, R.A.4    Michon, F.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.