Correlation of lymphocyte proliferating cell nuclear antigen expression with dietary cow's milk antigen load in infants with allergy to cow's milk

Citation
Ng. Papadopoulos et al., Correlation of lymphocyte proliferating cell nuclear antigen expression with dietary cow's milk antigen load in infants with allergy to cow's milk, INT A AL IM, 119(1), 1999, pp. 64-68
Citations number
19
Categorie Soggetti
Immunology
Journal title
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
ISSN journal
10182438 → ACNP
Volume
119
Issue
1
Year of publication
1999
Pages
64 - 68
Database
ISI
SICI code
1018-2438(199905)119:1<64:COLPCN>2.0.ZU;2-J
Abstract
Background: Controversial results have been reported on the participation a nd diagnostic value of lymphocyte reactivity in cow's milk (CM) allergy. In this study, we used a specific nuclear marker to evaluate lymphocyte proli feration in IgE-mediated CM allergy in infants, and examine its relation wi th diets containing different CM antigen loads. Methods: Infants with IgE-m ediated CM allergy, as assessed by open provocation and RAST, were grouped according to their exclusive diet, either CM formulae, breast feeding, or h ydrolysed whey formulae. A group of non-atopic infants receiving CM was als o examined. Lymphocyte proliferation to B-lactoglobulin was evaluated by qu antitation of the proliferating cell nuclear antigen (PCNA) expression in p eripheral blood mononuclear cells, by flow cytometry. Immunophenotypic surf ace markers were also examined. Results: A marked difference of PCNA expres sion between CM-fed allergic infants and healthy controls was observed (p<0 .001). In this setting, PCNA expression greater than or equal to 10% was hi ghly specific and sensitive as a marker of CM allergy in CM-fed infants. Mo reover, a significant correlation (p<0.001) between antigen load and PCNA w as established in CM-allergic infants under different diets, higher values obtained with increasing antigen loads. In addition, within the group fed h ydrolyzed formulae, low-molecular-weight products resulted in marginally lo wer PCNA expression than higher-molecular-weight formulae. No differences i n immunophenotype were found, with the exception of a higher CD23 expressio n in the breast-fed group. Conclusions: PCNA could be a useful marker in th e assessment of lymphocyte proliferation to CM antigens. Low CM antigen die ts are related with reduced lymphocyte reactivity, which may partly explain the clinical benefit observed with such diets.