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yet</button><a id="jr-fip-next" class="wsprkl btn" title="Jump to next match">▶</a></nav></nav></div><div id="jr-epub-interstitial" class="hidden"></div><div id="jr-content"><article data-type="main"><div class="main-content lit-style" itemscope="itemscope" itemtype="http://schema.org/CreativeWork"><div class="meta-content fm-sec"><div class="fm-sec"><h1 id="_NBK22199_"><span class="title" itemprop="name">Alpha-1-antitrypsin deficiency</span></h1><p class="fm-aai"><a href="#_NBK22199_pubdet_">Publication Details</a></p></div></div><div class="body-content whole_rhythm" itemprop="text"><p>Alpha-1-antitrypsin (AAT) is a protein that protects the body from damage by its immune cells. Deficiency of this protein leaves the lung, and occasionally the liver, vulnerable to injury.</p><p>The lung contains many tiny air sacs called alveoli. Oxygen travels across their walls into the bloodstream.</p><div class="iconblock whole_rhythm clearfix ten_col fig" id="figaatFigure" co-legend-rid="figlgndaatFigure"><a href="/books/NBK22199/figure/aatFigure/?report=objectonly" target="object" title="Lung alveoli" class="img_link icnblk_img figpopup" rid-figpopup="figaatFigure" rid-ob="figobaatFigure"><img class="small-thumb" src="/books/NBK22199/bin/aat.gif" src-large="/books/NBK22199/bin/aat.jpg" alt="Lung alveoli. In AAT deficiency, the walls of the lung tissue (alveoli) are broken down." /></a><div class="icnblk_cntnt" id="figlgndaatFigure"><h4 id="aatFigure"><a href="/books/NBK22199/figure/aatFigure/?report=objectonly" target="object" rid-ob="figobaatFigure">Lung alveoli</a></h4><p class="float-caption no_bottom_margin">In AAT deficiency, the walls of the lung tissue (alveoli) are broken down. The result is a trapping of air known as emphysema. The damaged lung tissue can no longer transfer oxygen to the bloodstream. </p></div></div><p>White blood cells release elastase, a powerful enzyme that can fight infections. But it can also attack normal tissues. If uncontrolled elastase is released around alveoli, it would destroy their walls and surrounding tissue, leaving areas of trapped air. This abnormal accumulation of air in the lungs is called emphysema and causes shortness of breath.</p><p>AAT inhibits elastase around normal tissue. Deficiency is caused by mutations in the SERPINA1 gene, located on chromosome 14. This gene has many different versions (alleles) that produce different amounts of AAT. The M allele produces normal levels of the AAT protein, the S allele produces moderately low levels, and the Z allele produces very low levels.</p><p>The alleles are expressed in a codominant manner — that means that a person with MZ has levels of AAT that are between the levels of those people who have alleles MM or ZZ. </p><p>Individuals who have at least one normal allele (MZ or MS) or two copies of S (SS) usually produce enough AAT to protect the lungs but do have an increased risk of lung disease. The risk is particularly high if they smoke. Individuals who inherit the Z allele from each parent (ZZ) have very low AAT and are at a higher risk of developing emphysema and liver disease.</p><p>There are over 70 known mutations that occur at the SERPINA1 gene. A common mutation that creates the Z allele involves a switch in amino acids — glutamic acid is replaced by lysine at position 342 (Glu342Lys). The resulting AAT protein cannot fold properly. This hinders its secretion from the liver (which makes AAT) into the bloodstream (which transports AAT to the lungs). The accumulation of AAT complexes can damage the liver, whereas the lack of AAT fails to stop the destruction of lung tissue.</p><p>Treatment of AAT deficiency includes the standard treatment of emphysema (bronchodilators, early use of antibiotics in infections) as well as the more experimental therapies of correcting AAT levels by replacing the protein. Gene therapy to replace the defective SERPINA1 gene with a functional copy is currently being investigated.</p><p>However, the most important part of treatment of AAT deficiency is to avoid smoking. Affected individuals are far less likely to develop emphysema if they do not smoke. Not only is smoking a lung irritant, which attracts white blood cells (and therefore neutrophil elastase) to the lungs, it also prevents any AAT that is present in the lungs from working properly.</p><div id="alpha1antitrypsindeficiency.disease-categories"><h2 id="_alpha1antitrypsindeficiency_disease-categories_">Related diseases</h2><ul class="simple-list"><li class="half_rhythm"><div>
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<a href="/books/n/gnd/A88/?report=reader">See other Respiratory Diseases</a>
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</div></li></ul></div><div id="bk_toc_contnr"></div></div></div><div class="fm-sec"><h2 id="_NBK22199_pubdet_">Publication Details</h2><h3>Publication History</h3><p class="small">Last Update: <span itemprop="dateModified">January 31, 2011</span>.</p><h3>Copyright</h3><div><div class="half_rhythm"><a href="/books/about/copyright/">Copyright Notice</a></div></div><h3>Publisher</h3><p><a href="https://www.ncbi.nlm.nih.gov/" ref="pagearea=page-banner&targetsite=external&targetcat=link&targettype=publisher">National Center for Biotechnology Information (US)</a>, Bethesda (MD)</p><h3>NLM Citation</h3><p>National Center for Biotechnology Information (US). Genes and Disease [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1998-. Alpha-1-antitrypsin deficiency. [Updated 2011 Jan 31].<span class="bk_cite_avail"></span></p></div><div class="small-screen-prev"><a href="/books/n/gnd/adrenoleukodystrophy/?report=reader"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 100 100" preserveAspectRatio="none"><path d="M75,30 c-80,60 -80,0 0,60 c-30,-60 -30,0 0,-60"></path><text x="20" y="28" textLength="60" style="font-size:25px">Prev</text></svg></a></div><div class="small-screen-next"><a href="/books/n/gnd/alportsyndrome/?report=reader"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 100 100" preserveAspectRatio="none"><path d="M25,30c80,60 80,0 0,60 c30,-60 30,0 0,-60"></path><text x="20" y="28" textLength="60" style="font-size:25px">Next</text></svg></a></div></article><article data-type="fig" id="figobaatFigure"><div id="aatFigure" class="figure bk_fig"><div class="graphic"><img data-src="/books/NBK22199/bin/aat.jpg" alt="Lung alveoli. In AAT deficiency, the walls of the lung tissue (alveoli) are broken down." /></div><h3><span class="label">Lung alveoli</span></h3><div class="caption"><p>In AAT deficiency, the walls of the lung tissue (alveoli) are broken down. The result is a trapping of air known as emphysema. The damaged lung tissue can no longer transfer oxygen to the bloodstream.</p></div></div></article></div><div id="jr-scripts"><script src="/corehtml/pmc/jatsreader/ptpmc_3.22/js/libs.min.js"> </script><script src="/corehtml/pmc/jatsreader/ptpmc_3.22/js/jr.min.js"> </script></div></div>
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