Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Pradip K. Maiti"'
Autor:
Howard A. Kaplan, Angela Aftanas, Darren Fast, Bram Ramjiawan, Michael B. Jackson, Henry H. Mantsch, Pradip K. Maiti
Publikováno v:
Cancer. 89:1134-1144
BACKGROUND A single chain antibody fragment, NovoMAb-G2-scFv, derived from a human anti-tumor monoclonal antibody recognizes tumor antigen molecules expressed on a wide variety of human cancers including melanoma, breast carcinoma, colon adenocarcino
Autor:
Pradip K. Maiti, Howard A. Kaplan, Michael D. Dan, G. Yancey Gillespie, William C. Halliday, Ashok K. Prashar, Xuanmin He, Albert D. Friesen
Publikováno v:
Journal of Neuro-Oncology. 35:93-100
The present study was undertaken to determine thepattern of immunoreactivity of BT32/A6, a human IgMmonoclonal antibody (MAb), with the following histological panels:1) 30 human and non-human cell lines, 2)32 normal human tissues, and 3) 28 tumorsof
Autor:
Ashok K. Prashar, Pradip K. Maiti, Mark C. Griffin, Elizabeth M. Earley, Howard A. Kaplan, Michael D. Dan, Albert D. Friesen, Xin Y. Yuan
Publikováno v:
Journal of Neurosurgery. 82:475-480
✓ The purpose of this study was to ascertain how various growth parameters may influence the labeling of SK-MG-1, a human glioma cell line, by BT32/A6, a human immunoglobulin M monoclonal antibody (MAb). By growing SKMG-1 cells at different culture
Autor:
Alec H. Sehon, Masaru Takata, Danuta Kierek-Jaszczuk, Soji Bitoh, V. Holford-Strevens, Pradip K. Maiti
Publikováno v:
Cellular Immunology. 150:168-193
We had previously shown (i) that conjugates of a given antigen A (AgA) and monomethoxypolyethylene glycol (mPEG) induced AgA-specific tolerance in mice which was mediated by polyclonal CD8+ suppressor T (Ts) cells, as well as by soluble factor(s) of
Autor:
Howard A. Kaplan, Michael B. Jackson, Bram Ramjiawan, Henry H. Mantsch, Pradip K. Maiti, Darren Fast
This study demonstrates the potential of in vivo, whole body fluorescence imaging for pharmacokinetic studies. The distribution of a novel human anti-tumour antibody fragment, NovoMab-G2-scFv, labelled with a fluorescent dye (Cy5.5.18) was monitored
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48605ccae6ab2f369aafe1266f4714c1
https://nrc-publications.canada.ca/eng/view/object/?id=d8672d57-a496-435a-bb7c-0729970c27c7
https://nrc-publications.canada.ca/eng/view/object/?id=d8672d57-a496-435a-bb7c-0729970c27c7
Autor:
Pradip K. Maiti, Edgar G. Engleman, Jeffrey P. Lake, John I. Magnani, Judith A. Kapp, Wayne R. Godfrey, Carl W. Pierce, Alec H. Sehon, Satoshi Fukuse, Bruce H. Devens, David R. Webb
Publikováno v:
International immunology. 7(8)
Although reliable antibodies are available that distinguish human suppressor T (Ts) cells from CTL and other T cells, few are available for murine Ts cells. We have developed a mAb (984D4.6.5) that, in the presence of complement, depletes alloantigen
Publikováno v:
Cellular immunology. 142(1)
The induction of antigen-specific tolerance in mice by conjugates of ovalbumin (OVA) and monomethoxypolyethylene glycol (mPEG) previously had been shown to be associated with the generation of antigen-specific suppressor T (Ts) cells. For the elucida
Autor:
Alec H. Sehon, Glen M. Lang, Danuta Kierek-Jaszczuk, Soji Bitoh, V. Holford-Strevens, Masaru Takata, Youhai H. Chen, Pradip K. Maiti
Publikováno v:
Cellular immunology. 137(1)
The findings of previous studies in this laboratory demonstrating that conjugates of human monoclonal (myeloma) IgG (HIgG) and monomethoxypolyethylene glycol (mPEG) were able to induce in mice antigen-specific tolerance and CD8+ suppressor T (Ts) cel
Publikováno v:
International Journal of Cancer. 41:17-22
The therapeutic effectiveness of xenogeneic monoclonal antibodies (MAbs) (xIg) or their conjugates with toxins (xIg-Tx) is undermined because of their inherent immunogenicity. This complication may be overcome by converting the antigenic xIg to toler
Publikováno v:
Mycopathologia. 91(2)
The role of humoral antibodies and the effect of BCG vaccination were studied in the experimental candidiasis in mice. The antibody suppressed, B-cell deficient animals were prepared by repeated administration of rabbit anti-mouse-mu-antiserum to the