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C
URRENT
O
PINION
Autophagy and role in asthma
Soma S.S.K. Jyothula
a
and N. Tony Eissa
b
Purpose of review
Asthma is a common worldwide respiratory illness with significant morbidity and mortality. The disease is
characterized by airway inflammation with involvement of multiple biological pathways. Genetic
predisposition and increased susceptibility to severe respiratory viral infections are well known clinical
features of asthma. Autophagy is an evolutionarily conserved cellular degradation process with significant
impact on immunity and antiviral response. In this review we have described the role of autophagy in
immune cell survival, proliferation and function. Autophagy has complex effects on immune response
involved in inflammation, specifically Th2 immune response. Common respiratory viruses are associated
with increased morbidity and mortality in asthmatic patients.
Recent findings
We describe recent studies showing the effect of autophagy on replication and immune response to
common respiratory viruses. The role of autophagy in asthma has recently been investigated. Two studies
have been published describing the association of autophagy with asthma. Genetic polymorphism in
specific autophagy genes is associated with asthma and influences gene expression in an experimental
in-vivo model.
Summary
These studies provide us with a window into the possible role of autophagy in asthma and offer new clues
to pathogenesis. Modulation of autophagy has the potential to develop into a new therapeutic avenue to
treat this common respiratory ailment.
Keywords
asthma, autophagy, common respiratory viruses, genetic polymorphism
INTRODUCTION
Asthma is a chronic respiratory illness caused by
chronic airway inflammation. In the USA, the pre-
valence of asthma was 8.2% (24.6 million persons)
in 2009. Prevalence among children (persons aged
<18 years) was 9.6%, and among adults was 7.7%
[1]. It is a complex disease with multiple known
associated triggers and is classified into various
clinical phenotypes (allergic asthma, work-related
asthma). The biological and pathological pathways
involved are myriad with no single process explain-
ing the disease process completely.
ASTHMA: ROLE OF ADAPTIVE AND
INNATE IMMUNITY
Airway inflammation is the most accepted paradigm
in the pathogenesis of asthma. The role of adaptive
immunity in airway inflammation has been studied
extensively. The adaptive immune response is anti-
gen-dependent and T helper cells (CD4
þ
) play a role
in execution. The two major T helper pathways (Th1
and Th2) are characterized by the cytokine profiles
(Th1 – IFN-g, TNF-b; Th2 – IL-4, IL-5, IL-10 and
IL-13). Th2 immune response is crucial in asthma
based on murine models and biological samples
from asthmatic patients. Asthma arises from an
imbalance between Th1 and Th2 pathways; over-
driven Th2 inflammation leads to airway inflam-
mation and asthma.
Innate immunity is an ancient conserved
immune response to infectious agents by recog-
nition of pathogen-associated molecular patterns
(PAMPs) and acts as the first immune barrier. Unlike
the adaptive immune response, it is rapid, antigen
processing is not required and memory is not gener-
ated. A number of immune and nonimmune cells in
a
Department of Medicine, The Methodist Hospital/Weill Cornell Medical
College and
b
Baylor College of Medicine, Houston, Texas, USA
Correspondence to Soma S.S.K. Jyothula, Department of Medicine, The
Methodist Hospital/Weill Cornell Medical College, 6550 Fannin St,
SM1001 Houston, TX 77030, USA. Tel: +1 713 441 2104; fax: +1
713 791 5043; e-mail: ssjyothula@tmhs.org
Curr Opin Pulm Med 2013, 19:30–35
DOI:10.1097/MCP.0b013e32835b1150
www.co-pulmonarymedicine.com Volume 19 Number 1 January 2013
REVIEW