R. Pawankar et Cs. Ra, HETEROGENEITY OF MAST-CELLS AND T-CELLS IN THE NASAL-MUCOSA, Journal of allergy and clinical immunology, 98(6), 1996, pp. 248-262
Allergic diseases like atopic rhinitis, bronchial asthma, and urticari
a are prevalent and on the rise. The need to better understand the pat
hophysiology of these diseases is therefore crucial to the development
of newer and more effective modes of treatment. We hypothesized that
in inflammatory diseases like allergic rhinitis and asthma characteriz
ed by profound local clinical manifestations and inflammation of the r
elevant mucosae, the most important immunopathological findings must o
ccur locally. Although studies on the cellular elements and mediators
in the peripheral blood compartment may provide useful information, th
ey may not accurately reflect events occurring within the target organ
itself. Even in the normal mucosa there is a resident population of l
ymphocytes and mast cells. Taking perennial allergic rhinitis (PAR) an
d chronic infective rhinitis (CIR) as representative chronic airway in
flammatory diseases we investigated the phenotypic and functional char
acteristics of most cell and lymphocytes in the nasal mucosa of patien
ts with PAR CIR during the natural course of the disease. We further c
ompared the characteristics of lymphocytes in the nasal mucosa with th
at in the peripheral blood compartment. our results demonstrated heter
ogeneity of mast cells and T cells in the nasal mucosa. Furthermore, t
he mucosal changes at the site of allergic inflammation were character
ized by an increase in the proportion of CD4(+) CD45RO(+) T cells (mem
ory cells); oligoclonal expansion and activation of V gamma 1/V delta
1(+) T cells; and increased number of Fc epsilon RI(+) cells; an incre
ased proportion of T-H2- type cytokine expressing mast cells and lymph
ocytes and of very late antigen-4 and very late antigen-5 expressing n
asal mast cells, independent of alterations in CIR; and autologous per
ipheral blood. these findings strongly suggest heterogeneity of lympho
cytes and mast cells in the nasal mucosa based on the underlying infla
mmatory disease, and compartmentalization of inflammatory cells in the
nasal mucosa and peripheral blood.