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C. pneumoniae IgA
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Chlamydophila pneumoniae IgA

Chlamydia pneumoniae is a common intracellular bacterial pathogen causing a range of respiratory infections such as pneumonia, bronchitis, sinusitis, and pharyngitis. 

It is widely prevalent globally, transmitted through respiratory routes, and has a high reinfection rate throughout life. 

While often asymptomatic or mildly symptomatic, C. pneumoniae can lead to severe respiratory illnesses in about 30% of cases. 

Beyond respiratory infections, it has been implicated in chronic conditions like asthma, chronic obstructive pulmonary disease (COPD), and even cardiovascular diseases such as atherosclerosis and coronary heart disease. 

The bacterium's persistence in the body, despite antibiotic treatment, poses significant challenges, necessitating further research into its pathogenesis and effective treatment strategies. 

IgA antibody testing for C. pneumoniae is valuable for diagnosing chronic respiratory infections, particularly in patients with COPD, where sputum IgA antibodies show good sensitivity and specificity. 

Elevated IgA antibody titers are linked to increased respiratory symptoms, decreased lung function, and higher mortality risk from ischemic heart disease, even after adjusting for conventional cardiovascular risk factors.

Chlamydophila pneumoniae: An Overview

Chlamydophila pneumoniae is a common intracellular bacterial respiratory pathogen with a unique biphasic life cycle [7.].

It is widely distributed globally and transmitted from human to human via the respiratory route, infecting the majority of the world's population; it has a high prevalence of reinfection throughout life [1., 7.].

C. pneumoniae causes about 10% of community-acquired pneumonia and 5% of pharyngitis, bronchitis, and sinusitis [2.].

In Western countries, new infections are most common between ages 5 and 15, and seroprevalence is higher in adult males [1.].

Most infections (70%) are asymptomatic or mildly symptomatic, but about 30% can cause severe respiratory illnesses [7.].

C. pneumoniae can cause various respiratory illnesses, including pneumonia, bronchitis, sinusitis, and pharyngitis [7.].

After an acute infection, C. pneumoniae can persist in a form that is resistant to antibiotics and potentially contributes to chronic respiratory conditions such as asthma, chronic bronchitis, and COPD [7.].

Additionally, evidence suggests a potential link between C. pneumoniae infection and atherosclerosis as the bacterium has been found in atherosclerotic plaques. It is also associated with coronary heart disease and acute myocardial infarction [1.]. 

It has also been implicated in other conditions like erythema nodosum and sarcoidosis [2.].

Naming and Classification of C. pneumoniae [9., 11.] 

Chlamydia pneumoniae is part of the Chlamydiae order, which contains obligate intracellular pathogens. 

The order initially comprised one genus, Chlamydia, with four recognized species: C. trachomatis, C. psittaci, C. pneumoniae, and C. pecorum. 

Recent taxonomic analysis has led to a proposed reclassification, suggesting the division of the genus Chlamydia into two genera: Chlamydia and Chlamydophila. 

Under this new classification, C. trachomatis would be joined by two new species, Chlamydia muridarum and Chlamydia suis. 

The genus Chlamydophila would include C. pecorum, C. pneumoniae, and C. psittaci, along with three new species derived from C. psittaci: Chlamydophila abortus, Chlamydophila caviae, and Chlamydophila felis. Despite ongoing controversy regarding this reclassification, the term Chlamydia is still commonly used.

Chlamydia pneumoniae, also known as TWAR, is distinguished from C. trachomatis and C. psittaci by its unique elementary body morphology and less than 10% DNA homology. 

Symptoms of Chlamydophila pneumoniae [1., 2., 8., 9.]

The symptoms of C. pneumoniae infections are similar to those caused by other respiratory pathogens but often present a subacute onset with pharyngitis that may resolve before bronchitis or pneumonia develops. A prolonged cough and slow recovery, even with antibiotic therapy, are common.

Diseases and Health Implications of C. pneumoniae

C. pneumoniae is associated with the following conditions: 

Respiratory Infections [2., 7.] 

  • Pneumonia
  • Bronchitis
  • Sinusitis 

Cardiovascular Diseases

  • Atherosclerosis [1.]
  • Coronary artery disease [1.] 
  • Myocardial infarction [1., 2.] 

Neurological Disorders

  • Multiple sclerosis [4.] 
  • Alzheimer's disease [4.] 

Chronic Respiratory Conditions

  • Exacerbation of asthma [7.] 
  • Chronic obstructive pulmonary disease (COPD) [7.]

Other Potential Associations

  • Arthritis [5.] 
  • Lung cancer [5.] 
  • Sarcoidosis [2.] 
  • Erythema Nodosum [2.] 

General Notes

  • Chlamydia pneumoniae can lead to severe infections, particularly in older individuals.
  • Further research is required to understand its pathogenesis and treatment strategies.

Clinical Significance of C. pneumoniae IgA Antibodies

IgA antibody testing for C. pneumoniae has shown clinical significance in diagnosing chronic respiratory infections. 

Studies have found that sputum IgA antibodies are present in a high percentage of patients with chronic obstructive pulmonary disease (COPD), with good sensitivity and specificity compared to serum antibody levels [16.]. 

Elevated IgA antibody titers have been associated with increased respiratory symptoms, including asthma and chronic bronchitis, as well as decreased lung function [6.].

Furthermore, IgA antibodies have been linked to increased mortality risk, particularly from ischemic heart disease, even after adjusting for conventional cardiovascular risk factors [14.].

Overall, IgA antibody testing appears to be a valuable tool for identifying persistent C. pneumoniae infections and associated health risks.

Laboratory Testing for Chlamydophila Pneumoniae IgA Antibodies

Test Information, Sample Collection and Preparation

C. pneumoniae is often tested by assessing the presence of antibodies against this organism.  Often, IgG, IgM, and IgA antibody levels are tested.

Interpretation of C. pneumoniae IgA Test Results

Serology tests can describe the timeline of infection, with the presence of IgM antibodies indicating a current or recent infection, and IgG antibodies indicating a past infection. IgA antibodies typically confirm an immune response in mucosal tissue, often from the respiratory or digestive tract.

IgA antibody testing for C. pneumoniae aids in diagnosing chronic respiratory infections. 

Studies have shown that sputum IgA antibodies are frequently present in patients with chronic obstructive pulmonary disease (COPD), demonstrating good sensitivity and specificity compared to serum antibody levels [16.].

Elevated IgA antibody titers are associated with increased respiratory symptoms, such as asthma and chronic bronchitis, and decreased lung function [6.].

Additionally, IgA antibodies are linked to a higher mortality risk, particularly from ischemic heart disease, even after adjusting for conventional cardiovascular risk factors [14.].

Overall, IgA antibody testing is a valuable tool for identifying persistent C. pneumoniae infections and their associated health risks.

Treatment of C. pneumoniae [8.]

Antimicrobial treatment of C. pneumoniae often consists of:

  • Erythromycin
  • Azithromycin (Zithromax®)
  • Clarithromycin (Biaxin®)
  • Levofloxacin (Levaquin®)
  • Moxifloxacin (Avelox®)

Each of these has shown 70-90% success in eradicating C. pneumoniae from the respiratory tract in cases of pneumonia.

Macrolides, ketolides, tetracyclines, quinolones, and rifamycins have all shown effectiveness in vitro [8.].

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See References

[1.] Blasi F, Tarsia P, Arosio C, Fagetti L, Allegra L. Epidemiology of Chlamydia pneumoniae. Clinical Microbiology and Infection. 1998;4:4S1-4S6. doi:https://doi.org/10.1111/j.1469-0691.1998.tb00697.x

[2.] Campbell LA, Kuo CC, Grayston JT. Chlamydia pneumoniae and cardiovascular disease. Emerg Infect Dis. 1998 Oct-Dec;4(4):571-9. doi: 10.3201/eid0404.980407. PMID: 9866733; PMCID: PMC2640250.

[3.] CDC. Laboratory Testing for Chlamydia pneumoniae. Chlamydia pneumoniae Infection. Published 2024. Accessed August 6, 2024. https://www.cdc.gov/cpneumoniae/php/laboratories 

[4.] Cheok YY, Lee CYQ, Cheong HC, Looi CY, Wong WF. Chronic Inflammatory Diseases at Secondary Sites Ensuing Urogenital or Pulmonary Chlamydia Infections. Microorganisms. 2020;8(1):127. doi:https://doi.org/10.3390/microorganisms8010127

[5.] Choroszy−Król I, Frej−Mądrzak M, Hober M, Jolanta Sarowska, Agnieszka Jama-Kmiecik. Infections Caused by Chlamydophila pneumoniae. Advances in Clinical and Experimental Medicine. 2014;23(1):123-126. doi:https://doi.org/10.17219/acem/37035

[6.] Falck G, Gnarpe J, Hansson LO, Sva¨rdsudd K, Gnarpe H. Comparison of Individuals with and Without Specific IgA Antibodies to Chlamydia pneumoniae. Chest. 2002;122(5):1587-1593. doi:https://doi.org/10.1378/chest.122.5.1587

[7.] Hahn DL, Azenabor AA, Beatty WL, Byrne GI. Chlamydia pneumoniae as a respiratory pathogen. Frontiers in Bioscience: A Journal and Virtual Library. 2002;7:e66-76. doi:https://doi.org/10.2741/hahn

[8.] Hammerschlag MR. Advances in the management of Chlamydia pneumoniae infections. Expert Review of Anti-infective Therapy. 2003;1(3):493-503. doi:https://doi.org/10.1586/14787210.1.3.493

[9.] Hammerschlag MR. Chlamydia trachomatis and Chlamydia pneumoniae Infections in Children and Adolescents. Pediatrics in Review. 2004;25(2):43-51. doi:https://doi.org/10.1542/pir.25-2-43

[10.] Kumar S, Saigal SR, Sethi GR. Detection of IgM and IgG antibodies to Chlamydophila pneumoniae in pediatric community-acquired lower respiratory tract infections. Indian J Pathol Microbiol. 2011 Oct-Dec;54(4):782-5. doi: 10.4103/0377-4929.91501. PMID: 22234110.

[11.] Kuo CC, Jackson LA, Campbell LA, Grayston JT. Chlamydia pneumoniae (TWAR). Clinical Microbiology Reviews. 1995;8(4):451-461. doi:https://doi.org/10.1128/CMR.8.4.451

[12.] Miyashita N, Kawai Y, Tanaka T, et al. Antibody responses of Chlamydophila pneumoniae pneumonia: Why is the diagnosis of C. pneumoniae pneumonia difficult? Journal of Infection and Chemotherapy. 2015;21(7):497-501. doi:https://doi.org/10.1016/j.jiac.2015.03.003

‌[13.] Peeling RW. Laboratory diagnosis of Chlamydia pneumoniae infections. Can J Infect Dis. 1995 Jul;6(4):198-203. doi: 10.1155/1995/696950. PMID: 22514397; PMCID: PMC3327923.‌

[14.] Strachan DP, Carrington D, Mendall MA, et al. Relation of Chlamydia pneumoniae serology to mortality and incidence of ischaemic heart disease over 13 years in the Caerphilly prospective heart disease study   Commentary: Chlamydia pneumoniae infection and ischaemic heart disease. BMJ. 1999;318(7190):1035-1040. doi:https://doi.org/10.1136/bmj.318.7190.1035

[15.] Tuuminen T, Salo K, Surcel HM. A casuistic immunologic response in primary and repeated Chlamydophila pneumoniae infections in an immunocompetent individual. J Infect. 2002 Oct;45(3):202-6. doi: 10.1016/s0163-4453(02)91021-2. PMID: 12387780.

[16.] von Hertzen L, Leinonen M, Surcel HM, J Karjalainen, P Saikku. Measurement of sputum antibodies in the diagnosis of acute and chronic respiratory infections associated with Chlamydia pneumoniae. Clinical and diagnostic laboratory immunology. 1995;2(4):454-457. doi:https://doi.org/10.1128/cdli.2.4.454-457.1995

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