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Measurement of Humoral Immune Competence and the Risk of Sinopulmonary Infection in a Cohort of Kidney Transplant Recipients
Authors:C. Dendle  R.L. Stuart  W.R. Mulley  K.R. Polkinghorne  P.Y. Gan  J. Kanellis  J. Ngui  K. Laurie  K. Thursky  V.K. Leung  S.R. Holdsworth
Affiliation:1. Centre for Inflammatory Diseases, School of Clinical Sciences, Monash University, Clayton, Victoria, Australia;2. Monash Infectious Diseases, Monash Health, Clayton, Victoria, Australia;3. Department of Nephrology, Monash Medical Centre, Clayton, Victoria, Australia;4. Department of Epidemiology and Preventive Medicine, Monash University, Prahran, Victoria, Australia;5. Department of Immunology, Monash Pathology, Monash Health, Clayton, Victoria, Australia;6. WHO Collaborating Centre for Reference and Research on Influenza, Victorian Infectious Diseases Reference Laboratory at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia;7. School of Applied and Biomedical Sciences, Federation University, Churchill, Victoria, Australia;8. Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Victoria, Australia;9. National Centre for Infections in Cancer, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
Abstract:

Purpose

The aim of this study was to determine if measurement of B cell protective immunity was associated with susceptibility to sinopulmonary infection in kidney transplant recipients.

Methods and Materials

A prospective cohort of 168 patients with stable graft function (median 4.1 years) underwent assessment of B-lymphocyte antigen CD19 (CD19+) cell number, immunoglobulin G concentration, and seroresponses to influenza vaccination upon study entry. Patients received a single dose of a trivalent, seasonal influenza vaccine.

Results

After 2 years follow-up, 31 patients (18%) developed sinopulmonary infection. CD19+ cell number was strongly associated with future sinopulmonary infection. A higher proportion of patients with CD19+ cell counts below the fifth percentile for controls developed sinopulmonary infections than those above the fifth percentile, 30% (23 of 77 patients) compared with 9% (7 of 79 patients; P = .001). There was a trend toward a higher proportion of patients with reduced immunoglobulin G concentrations developing infections than in the normal range for controls, 29% (14 of 48 patients) compared with 15% (16 of 108 patients; P = .060). Influenza vaccination seroresponses were poor in patients and controls such that they could not be used to identify a subgroup of patients at high risk for the development of severe pulmonary infection.

Conclusions

Monitoring B-cell numbers represents a simple, inexpensive means of stratifying transplant recipients' risk of sinopulmonary infection.
Keywords:Address correspondence to Claire Dendle   MBBS   Monash Infectious Diseases   Level 3   Monash Medical Centre   246 Clayton Rd   Clayton   Victoria   Australia 3168. Tel.: +61 3 95944564. Fax: +61 3 95944533.
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