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Volumn 6, Issue 5, 1994, Pages 707-714

Recent developments in immunotoxin therapy

Author keywords

[No Author keywords available]

Indexed keywords

IMMUNOTOXIN; RICIN A;

EID: 0028148350     PISSN: 09527915     EISSN: None     Source Type: Journal    
DOI: 10.1016/0952-7915(94)90073-6     Document Type: Article
Times cited : (44)

References (79)
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    • of special interest, This paper demonstrates that one way to decrease the immunogenicity of ITs is to modify them with PEG. In this paper, PEG was introduced in a conjugate consisting of human TGF and PE38. The PEG conjugate remained in the circulation two-fold longer and its immunogenicity was 5–10 times lower than that of non-pegylated conjugate.
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    • of special interest, PE35 is a mutant form of PE that does not require proteolysis for activity. When it was conjugated to different thiolated antibodies, the resulting ITs were several-fold more active than ITs containing PE38 or PE40 (which are bound through a protease-sensitive bond) and caused complete regression of human xenografts in nude mice.
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    • of special interest, A recombinant anti-Tac(Fv)-C3-PE38KDEL was purified employing receptor-affinity chromatography. The IT was highly effective in specifically killing cells bearing IL-2 receptors. It may be useful in preventing allograft rejection and the treatment of autoimmune diseases.
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    • of special interest, In this Phase I trial, 12 patients in complete remission after ABMT were treated with anti-B4-BLR for relapsed B-cell NHL.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.