| The Immunology Group at the
NCTCC has extensive experience in the development and production of
polyclonal and monoclonal antibodies. These can be produced to native
proteins, whole cells, synthetic peptides, recombinant / fusion proteins, or
drug metabolites. The group also carries out research at the highest
international level in collaborations with academic and clinical partners.
The Immunology Group collaborates with both academic and industrial
partners in the development of unique monoclonal antibodies. Monoclonal
antibodies to the multidrug resistance markers MDR-1, MDR-3, Topo IIa and
MRP1 have been developed at the NCTCC and are available commercially.
Research Areas:
- Monoclonal and polyclonal antibody development
- Evaluation of new MAbs in clinical samples
- The mechanism of multidrug resistance
- Clinical studies of candidate cancer markers
Selected Research Publications
Liang Y
et al., (2001). Selection with melphalan or paclitaxel (Taxol) yields
variants with different patterns of multidrug resistance, integrin
expression and in vitro invasiveness. Eur J Cancer 37: 1041-1052.
Larkin A et al., (1999). Preliminary immunocytochemical studies of MDR-1 and
MDR-3 Pgp expression in B-cell leukaemias. Adv Exp Med Biol 457: 65-70.
Larkin A et al., (1999). A new monoclonal
antibody that specifically recognises the MDR-3-encoded gene product. Int J
Cancer 80: 265-271.
Moran E et al., (1998). Monoclonal
antibodies raised to paraffin wax embedded archival tissue; feasibility
study of their potential to detect novel antigenic markers.J Immunol Methods
219: 151-159.
Moran E et al., (1997). A new mdr-1 encoded
P-170 specific monoclonal antibody: (6/1C) on paraffin wax embedded tissue
without pretreatment of sections. J Clin Pathol. 50: 465-471.
Moran E et al., (1997). Co-expression of
MDR-associated markers, including P-170, MRP and LRP and cytoskeletal
proteins, in three resistant variants of the human ovarian carcinoma cell
line, OAW42. Eur J Cancer 33: 652-660.
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