Immunology Publications
Translational research of diagnostic
techniques:
- Walshe, D., Gaspar, H.B., Thrasher, A.J., Cale, C.M. and
Gilmour, KC. (2009) Signal Transducer and activator of
transcription 5 tyrosine phosphorylation for the diagnosis and
monitoring of patients with severe combined immunodeficiency.J.
Allergy Clin. Immunol.123: 505-508.
- Wheeler, R.D., Cale, C.M., Cetica, V., Aricò, M. and
Gilmour, K.C. (2010) A novel assay for investigation of suspected
familial haemophagocytic lymphohistiocytosis.Brit. Journ.
Haematol.150: 727-729.
- Cetica, V., Santoro, A., Gilmour, K.C.,Sieni, E., Pende, D.,
Marcenaro, S., Koch, F., Grieve, S., Wheeler, R., Zhao, F., zur
Stadt, U.,Griffiths, G.M. and Arico, M. (2010) STXBP2 mutations in
children with familial haemophagocytic lymphohistiocytosis type 5.
J Med Genet. 47: 595-600.
Translational cell therapies:
- Chatziandreou, I.*, Gilmour, K.C.*,
McNicol, A-M, Costabile, M., Sinclair, J., Cubitt, D.,Campbell,
J.D.M., Kinnon, C., Qasim, W. and Gaspar, H.B. (2007 ) Capture and
Generation of Adenoviral Specific T cells for adoptive
immunotherapy.Br. J. Haematol 136:117-126.
- Qasim, W., Derniame, S., Gilmour, K., Chiesa, R., Weber, M.,
Adams, S., Rao, K., Amrolia, P., Goulden, N., Very, P. and Gaspar,
H. (2011) Third-party virus-specific T cells eradicate
adenoviraemia but trigger bystander graft-versus-host disease.Brit.
Journ. Haematol.154: 150-3.
Diagnostics and clinical outcome:
- Booth C, Gilmour KC, Veys P, et al. (2011) X-linked
lymphoproliferative disease due to SAP/SH2D1A deficiency: a
multicenter study on the manifestations, management and outcome of
the disease. Blood. 6;117(1):53-62.
- Speckman, C., Pannicke, U., Wiech, E., Schwarz, K., Fisch, P.,
Friedrich, W., Niehuess, T., Gilmour, K., Buiting, K., Schlesier,
M., Eibel, H., Rohr, J., Superti-Furga, A., Gross-Wieltsch U., Ehl,
S. (2008) Clinical and immunological consequences of a somatic
reversion in a patient with X-linked severe combined
immunodeficiency.Blood,112: 4090-4097.
- Yong, P., Post, F., Gilmour, K.C., King, A., Easterbrook, P.,
Ibrahim, M.A.A. (2008) Cerebral toxoplasmosis in a middle-aged man
as first presentation of primary immunodeficiency due to a
hypomorphic mutation in CD40 ligand geneJ. Clin Path,61:
1220-1222.
- Sharpe LR, Ancliff P, Amrolia P, Gilmour KC, Vellodi A. (2009)
Type II Gaucher disease manifesting as haemophagocytic
lymphohistiocytosis.J Inherit Metab Dis. #157 e-pub ahead of
print
Review:
- Gholam, C., Girgoriadous, S., Gilmour, K.C and Gaspar, H.B.
(2011) Familial haemophagocytic lymphohistiocytosis: advances in
the genetic basis, diagnosis and management.Clin. Exp. Immunol.163:
271-283.