Two new human herpesviruses have recently been described. The overall objective of this project is to better define their medical significance in immunocompromised patients in whom other herpesviruses are important pathogens.
Specific Aim 1 To collect serial samples from the patients and test for the presence of HHV6 and HHV7 using qualitative PCR, quantitative PCR and methods to type strains of virus.
Specific Aim 2 To use these virologic criteria to define infected patients so that the specificity and sensitivity of serologic methods for IgG antibodies can be determined.
Specific Aim 3 To analyse all of the results obtained to identify temporal associations between the presence of either virus and particular clinical syndromes. To determine if these syndromes are associated with greater amounts of virus detected by quantitative methods. To determine the prognostic value for future disease of detecting either virus qualitatively or quantitatively in a prospective manner.
Specific Aim 4 To determine whether infection or disease attributable to either virus is acquired from endogeneous reactivation of virus or from primary infection or reinfection from the donor organ in patients undergoing transplant. To determine if pre-existing immunity in the recipient can moderate the pathologic potential of these viruses. Overall, this project will define the medical significance of these new human herpesviruses for immunocompromised patients and will define when virus replication is at its highest so that trials of antiviral chemotherapy can be planned.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI033389-02
Application #
2068393
Study Section
Epidemiology and Disease Control Subcommittee 2 (EDC)
Project Start
1993-07-15
Project End
1996-06-30
Budget Start
1994-07-01
Budget End
1995-06-30
Support Year
2
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of London Institute of Neurology
Department
Type
DUNS #
City
London
State
Country
United Kingdom
Zip Code
Emery, V C (2001) Human herpesviruses 6 and 7 in solid organ transplant recipients. Clin Infect Dis 32:1357-60
Kidd, I M; Clark, D A; Emery, V C (2000) A non-radioisotopic quantitative competitive polymerase chain reaction method: application in measurement of human herpesvirus 7 load. J Virol Methods 87:177-81
Kidd, I M; Clark, D A; Sabin, C A et al. (2000) Prospective study of human betaherpesviruses after renal transplantation: association of human herpesvirus 7 and cytomegalovirus co-infection with cytomegalovirus disease and increased rejection. Transplantation 69:2400-4
Griffiths, P D; Ait-Khaled, M; Bearcroft, C P et al. (1999) Human herpesviruses 6 and 7 as potential pathogens after liver transplant: prospective comparison with the effect of cytomegalovirus. J Med Virol 59:496-501
Kidd, I M; Clark, D A; Bremner, J A et al. (1998) A multiplex PCR assay for the simultaneous detection of human herpesvirus 6 and human herpesvirus 7, with typing of HHV-6 by enzyme cleavage of PCR products. J Virol Methods 70:29-36
Fabio, G; Knight, S N; Kidd, I M et al. (1997) Prospective study of human herpesvirus 6, human herpesvirus 7, and cytomegalovirus infections in human immunodeficiency virus-positive patients. J Clin Microbiol 35:2657-9
Clark, D A; Kidd, I M; Collingham, K E et al. (1997) Diagnosis of primary human herpesvirus 6 and 7 infections in febrile infants by polymerase chain reaction. Arch Dis Child 77:42-5
Clark, D A; Ait-Khaled, M; Wheeler, A C et al. (1996) Quantification of human herpesvirus 6 in immunocompetent persons and post-mortem tissues from AIDS patients by PCR. J Gen Virol 77 ( Pt 9):2271-5
Kidd, I M; Clark, D A; Ait-Khaled, M et al. (1996) Measurement of human herpesvirus 7 load in peripheral blood and saliva of healthy subjects by quantitative polymerase chain reaction. J Infect Dis 174:396-401