Cytokines as adjuvants for the induction of mucosal immunity.

Abstract:

:Safe nasal vaccines capable of promoting both mucosal and systemic immunity are needed for effective protection against bacterial and viral pathogens. While parenteral cytokine treatment could lead to unwanted toxicity, the nasal delivery route results in low but biologically active serum cytokine levels. Interleukin (IL)-6, IL-1 and IL-12, which promote either Th2- or Th1-type responses, respectively, also enhance systemic immunity to co-administered antigens. The chemoattractants lymphotactin (Lptn), RANTES and defensins also exerted adjuvant activity for systemic immunity when nasally administered with antigens. However, each cytokine or innate factor promoted a distinct pattern of T helper cell responses and corresponding IgG subclass response. Interleukin-12, IL-1, and the chemokines Lptn and RANTES promote mucosal immunity. In contrast, nasal IL-6 and defensins failed to induce mucosal S-IgA Ab responses, suggesting that mechanisms more complex than T cell activation and chemotaxis are required for the development of mucosal immunity after nasal delivery of cytokines.

journal_name

Adv Drug Deliv Rev

authors

Boyaka PN,McGhee JR

doi

10.1016/s0169-409x(01)00170-3

subject

Has Abstract

pub_date

2001-09-23 00:00:00

pages

71-9

issue

1-3

eissn

0169-409X

issn

1872-8294

pii

S0169-409X(01)00170-3

journal_volume

51

pub_type

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