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C. pneumoniae IgG
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Chlamydophila pneumoniae IgG

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. 

IgG antibodies against Chlamydophila pneumoniae are crucial in diagnosing and managing respiratory and cardiovascular conditions, with studies showing a strong association between these antibodies and cardiovascular disease.

These antibodies persist for months to years, indicating frequent reinfections and serving as important markers for both acute and chronic C. pneumoniae infections.

Chlamydophila pneumoniae: An Overview

Chlamydophila pneumoniae is a common intracellular bacterial respiratory pathogen with a unique biphasic life cycle [8.].

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., 8..].

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 [8.].

C. pneumoniae can cause various respiratory illnesses, including pneumonia, bronchitis, sinusitis, and pharyngitis [8.].

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 [8.].

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 [10., 12.] 

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., 9., 10.]

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., 8.] 

  • 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 [8.] 
  • Chronic obstructive pulmonary disease (COPD) [8.]

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 IgG Antibodies

IgG antibodies against Chlamydophila pneumoniae have significant clinical relevance in various respiratory and cardiovascular conditions. 

Studies have shown a strong association between IgG antibodies to C. pneumoniae and cardiovascular disease, with 94.3% of patients testing positive compared to 37% of healthy individuals [6.]

In peripheral arterial disease, specific IgG antibodies against 39 kDa and 54 kDa proteins were found to correlate with the presence of C. pneumoniae DNA [7.]

These antibodies may reflect an initial stage of infection, followed by an immunomediated response even in the absence of the bacteria [7.].

C. pneumoniae IgG antibodies can persist for months to years. Seroprevalence studies show 50-70% of adults have IgG antibodies, indicating frequent reinfections [11.].

Overall, IgG antibodies against C. pneumoniae serve as important markers for both acute and chronic infections, aiding in diagnosis and management of associated diseases.

Laboratory Testing for Chlamydophila Pneumoniae IgM 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 IgM 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.

Elevated IgG antibodies against Chlamydophila pneumoniae are clinically significant in diagnosing and managing various respiratory and cardiovascular conditions [6.].

Studies indicate a strong association between these antibodies and chronic respiratory infections as well as cardiovascular disease, with a high prevalence in affected patients compared to healthy individuals. [7., 11.]

IgG antibodies, which can persist for months to years, often reflect past infections and frequent reinfections, serving as important markers for both acute and chronic C. pneumoniae infections [13.].

Treatment of C. pneumoniae [9.]

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 [9.].

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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.] García-Elorriaga Gde L, Calderón-Abbo M, González-Bonilla CR. Asociación entre enfermedad cardiovascular y anticuerpos contra Chlamydia pneumoniae [Association between cardiovascular disease and anti-Chlamydia pneumoniae antibodies]. Salud Publica Mex. 2002 May-Jun;44(3):243-6. Spanish. PMID: 12132322.

[7.] Gutiérrez J, Linares J, Camacho A, Palanca M, Maroto C, Ros E, Luna JD, José Soto M, Sorlózano A. Descripción de inmunógenos de Chlamydia pneumoniae reconocidos por el suero de sujetos con enfermedad arterial periférica [Description of immunogens of Chlamydia pneumoniae recognized by serum of individuals with peripheral artery disease]. Med Clin (Barc). 2006 May 20;126(19):721-7. Spanish. doi: 10.1157/13088945. Erratum in: Med Clin (Barc). 2006 Oct 14;127(14):532. PMID: 16759586.

[8.] 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

[9.] 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

[10.] 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

[11.] 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.

[12.] 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

[13.] 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

[14.] 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.‌

[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.

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