Pneumocystis pneumonia

Not to be confused with Pneumococcal pneumonia.
Pneumocystis pneumonia
Pneumocystis jirovecii cysts from bronchoalveolar lavage, stained with Toluidine blue O stain
SpecialtyInfectious disease, pulmonology
CausesPneumocystis jirovecii[1]
Risk factorsWeakened immune system[1]
Differential diagnosisOther types of pneumonia
Medicationco-trimoxazole,[1] steroids, pentamidine, trimetrexate, dapsone, atovaquone, primaquine, pafuramidine maleate and clindamycin.

Pneumocystis pneumonia (PCP), also known as Pneumocystis jirovecii pneumonia (PJP), is a form of pneumonia caused by the fungus Pneumocystis jirovecii.[2][3]

Pneumocystis specimens are commonly found in the lungs of healthy people although it is usually not a cause for disease.[4] However, they are a source of opportunistic infection and can cause lung infections in people with a weak immune system or other predisposing health conditions. PCP is seen in people with HIV/AIDS (who account for 30-40% of PCP cases), those using medications that suppress the immune system, and people with cancer, autoimmune or inflammatory conditions, and chronic lung disease.[1]

Signs and symptoms

Signs and symptoms may develop over several days or weeks[1] and may include: shortness of breath and/or difficulty breathing (of gradual onset), fever, dry/non-productive cough, weight loss, night sweats,[5] chills, and fatigue.[1] Uncommonly, the infection may progress to involve other visceral organs (such as the liver, spleen, and kidney).[5]

  • Cough - typically dry/non-productive because sputum becomes too viscous to be coughed up. The dry cough distinguishes PCP from typical pneumonia.[5]

Complications

X-ray and CT of ground glass opacities and pneumothorax in pneumocystis pneumonia.[6]

Pneumothorax is a well-known complication of PCP.[7] Also, a condition similar to acute respiratory distress syndrome (ARDS) may occur in patients with severe Pneumocystis pneumonia, and such individuals may require intubation.[8]

Pathophysiology

The risk of PCP increases when CD4-positive T-cell levels are less than 400 cells/μL. In these immunosuppressed individuals, the manifestations of the infection are highly variable.[9] The disease attacks the interstitial, fibrous tissue of the lungs, with marked thickening of the alveolar septa and alveoli, leading to significant hypoxia, which can be fatal if not treated aggressively. In this situation, lactate dehydrogenase levels increase and gas exchange is compromised. Oxygen is less able to diffuse into the blood, leading to hypoxia, which along with high arterial carbon dioxide (CO
2) levels, stimulates hyperventilatory effort, thereby causing dyspnea (breathlessness).

In addition, in symptomatic cases of P. jirovecii pneumonia, the overgrowth of the fungus is associated to a co-infection with trichomonads, unicellular flagellated parabasalid protist (Parabasalia) of the family Trichomonadidae. These parasites (including the commensal Trichomonas tenax, Trichomonas vaginalis and Tritrichomonas foetus) exhibit an amoeboid form, without flagellum, which makes it difficult to identify them under the microscope.[10] Amoeboid transformation is an argument in favor of a deleterious action, which nevertheless remains conjectural.[11]

Diagnosis

The diagnosis can be confirmed by the characteristic appearance of the chest X-ray and an arterial oxygen level (PaO2) that is strikingly lower than would be expected from symptoms. Gallium 67 scans are also useful in the diagnosis. They are abnormal in about 90% of cases and are often positive before the chest X-ray becomes abnormal. Chest X-ray typically shows widespread pulmonary infiltrates. CT scan may show pulmonary cysts (not to be confused with the cyst-forms of the pathogen).

  • Chest X-ray demonstrating bilateral pulmonary infiltrates caused by pneumocystis pneumonia.
    Chest X-ray demonstrating bilateral pulmonary infiltrates caused by pneumocystis pneumonia.
  • Chest X-ray of increased opacification (whiteness) in the lower lungs.
    Chest X-ray of increased opacification (whiteness) in the lower lungs.
  • These chest radiographs are of two patients. Both show ground glass opacities. The left X-ray shows a much more subtle ground-glass appearance while the right X-ray shows a much more gross ground-glass appearance mimicking pulmonary edema.
    These chest radiographs are of two patients. Both show ground glass opacities. The left X-ray shows a much more subtle ground-glass appearance while the right X-ray shows a much more gross ground-glass appearance mimicking pulmonary edema.[6]
  • X-ray of a cyst in pneumocystis pneumonia
    X-ray of a cyst in pneumocystis pneumonia[6]
  • High-resolution computed tomography (HRCT) showing ground-glass attenuation with a geographic or mosaic distribution.
    High-resolution computed tomography (HRCT) showing ground-glass attenuation with a geographic or mosaic distribution.[6]
  • HRCT of cysts of pneumocystis pneumonia. These are usually multiple and bilateral, but range in size, shape and distribution.
    HRCT of cysts of pneumocystis pneumonia. These are usually multiple and bilateral, but range in size, shape and distribution.[6]

The diagnosis can be definitively confirmed by histological identification of the causative organism in sputum or bronchoalveolar lavage (lung rinse). Staining with toluidine blue, silver stain, periodic acid-Schiff stain, or an immunofluorescence assay shows the characteristic cysts.[12] The cysts resemble crushed ping-pong balls and are present in aggregates of two to eight (and not to be confused with Histoplasma or Cryptococcus, which typically do not form aggregates of spores or cells). A lung biopsy would show thickened alveolar septa with fluffy eosinophilic exudate in the alveoli. Both the thickened septa and the fluffy exudate contribute to dysfunctional diffusion capacity that is characteristic of this pneumonia.

Pneumocystis infection can also be diagnosed by immunofluorescent or histochemical staining of the specimen, and more recently by molecular analysis of polymerase chain reaction products comparing DNA samples. Notably, simple molecular detection of P. jirovecii in lung fluids does not mean that a person has PCP or infection by HIV. The fungus appears to be present in healthy individuals in the general population.[13] A blood test to detect β-D-glucan (a part of the cell wall of many different types of fungi) can also help in the diagnosis of PCP.

Prevention

In immunocompromised people, prophylaxis with co-trimoxazole (trimethoprim/sulfamethoxazole),[14] atovaquone, or regular pentamidine inhalations may help prevent PCP.

Treatment

Antipneumocystic medication is used with concomitant steroids to avoid inflammation, which causes an exacerbation of symptoms about 4 days after treatment begins if steroids are not used. By far, the most commonly used medication is trimethoprim/sulfamethoxazole, but some patients are unable to tolerate this treatment due to allergies. Other medications that are used, alone or in combination, include pentamidine, trimetrexate, dapsone, atovaquone, primaquine, pafuramidine maleate (under investigation), and clindamycin. Treatment is usually for a period of about 21 days. Pentamidine is less often used, as its major limitation is the high frequency of side effects. These include acute pancreatic inflammation, kidney failure, liver toxicity, decreased white blood cell count, rash, fever, and low blood sugar.

Epidemiology

Pneumocystis jirovecii

The disease PCP is relatively rare in people with normal immune systems, but common among people with weakened immune systems, such as premature or severely malnourished children, the elderly, and especially persons living with HIV/AIDS (in whom it is most commonly observed).[2][15] PCP can also develop in patients who are taking immunosuppressive medications. It can occur in patients who have undergone solid organ transplantation or bone marrow transplantation and after surgery.[16] Infections with Pneumocystis pneumonia are also common in infants with hyper IgM syndrome, an X-linked or autosomal recessive trait.

The causative organism of PCP is distributed worldwide[17] and Pneumocystis pneumonia has been described in all continents except Antarctica.[17] More than 75% of children are seropositive by the age of four, which suggests a high background exposure to the organism. A post mortem study conducted in Chile of 96 persons who died of unrelated causes (suicide, traffic accidents, and so forth) found that 65 (68%) of them had pneumocystis in their lungs, which suggests that asymptomatic pneumocystis infection is extremely common.[18] Up to 20% of adults may be asymptomatic carriers at any given time, and asymptomatic infection may persist for months before being cleared by an immune response.[1]

P. jirovecii is commonly believed to be a commensal organism (dependent upon its human host for survival). The possibility of person-to-person transmission has recently gained credence, with supporting evidence coming from many different genotyping studies of P. jirovecii isolates from human lung tissue.[19][20] For example, in one outbreak of 12 cases among transplant patients in Leiden, it was suggested as likely, but not proven, that human-to-human spread may have occurred.[21]

AIDS

Since the start of the AIDS epidemic, PCP has been closely associated with AIDS. Because it only occurs in an immunocompromised host, it may be the first clue to a new AIDS diagnosis if the patient has no other reason to be immunocompromised (e.g. taking immunosuppressive drugs for organ transplant). An unusual rise in the number of PCP cases in North America, noticed when physicians began requesting large quantities of the rarely used antibiotic pentamidine, was the first clue to the existence of AIDS in the early 1980s.[22][23]

Prior to the development of more effective treatments, PCP was a common and rapid cause of death in persons living with AIDS. Much of the incidence of PCP has been reduced by instituting a standard practice of using oral co-trimoxazole (Bactrim / Septra) to prevent the disease in people with CD4 counts less than 200/μL. In populations who do not have access to preventive treatment, PCP continues to be a major cause of death in AIDS.

History

The first cases of Pneumocystis pneumonia were described in premature infants in Europe following the Second World War.[24] It was then known as plasma cellular interstitial pneumonitis of the newborn.[24]

In the era before the existence of HIV/AIDS in humans, clinical transplant immunology, and widespread immunomodulatory therapy for autoimmune diseases, the neonatal and infantile population was the principal immunity-limited population. For example, a 1955 review article stated,[25] "Interstitial plasma cell pneumonia is a type of infantile pneumonia, occurring chiefly in Europe." It also stated, "The etiology is unknown, but the disease acts like an infection in its epidemiology. No present-day therapeutic measures seem to be of any definite value."[25]

Name

Both Pneumocystis pneumonia and pneumocystis pneumonia[26] are orthographically correct; one uses the genus name per se and the other uses the common noun based on it. (This is the same reason, for example, why "group A Streptococcus" and "group A streptococcus" are both valid.) Synonyms for PCP include pneumocystosis[26] (pneumocystis + -osis), pneumocystiasis[26] (pneumocystis + -iasis), and interstitial plasma cell pneumonia.[26]

The older species name Pneumocystis carinii (which now applies only to the Pneumocystis species that is found in rats[27]) is still in common usage. As a result, Pneumocystis pneumonia (PCP) is also known as Pneumocystis jiroveci[i] pneumonia and (incorrectly) as Pneumocystis carinii pneumonia.[28][29][30]

Regarding nomenclature, when the name of Pneumocystis pneumonia (PCP) changed from P. carinii pneumonia to P. jirovecii pneumonia, it was at first asked whether "PJP" should replace "PCP". However, because the short name "PCP" was already well established among physicians that managed patients with Pneumocystis infection, it was widely accepted that this name could continue to be used, as it could now stand for pneumocystis pneumonia.[31]

References

  1. 1 2 3 4 5 6 7 "Pneumocystis pneumonia | Fungal Diseases | CDC". www.cdc.gov. 2020-07-27. Archived from the original on 2021-07-26. Retrieved 2020-08-10.
  2. 1 2 Aliouat-Denis CM, Chabé M, Demanche C, Aliouat EM, Viscogliosi E, Guillot J, et al. (September 2008). "Pneumocystis species, co-evolution and pathogenic power". Infection, Genetics and Evolution. 8 (5): 708–726. doi:10.1016/j.meegid.2008.05.001. PMID 18565802.
  3. ↑ Bennett NJ, Gilroy SA (2017-08-08). "Pneumocystis jiroveci Pneumonia (PJP) Overview of Pneumocystis jiroveci Pneumonia". Medscape. Archived from the original on 2022-12-21. Retrieved 2023-01-29.
  4. ↑ Ponce CA, Gallo M, Bustamante R, Vargas SL (February 2010). "Pneumocystis colonization is highly prevalent in the autopsied lungs of the general population". Clinical Infectious Diseases. 50 (3): 347–353. doi:10.1086/649868. PMID 20047487.
  5. 1 2 3 "Pneumocystis Pneumonia". NORD (National Organization for Rare Disorders). Archived from the original on 2020-11-01. Retrieved 2020-08-10.
  6. 1 2 3 4 5 Allen CM, Al-Jahdali HH, Irion KL, Al Ghanem S, Gouda A, Khan AN (October 2010). "Imaging lung manifestations of HIV/AIDS". Annals of Thoracic Medicine. 5 (4): 201–216. doi:10.4103/1817-1737.69106. PMC 2954374. PMID 20981180. Creative Commons Attribution License
  7. ↑ Kanne JP, Yandow DR, Meyer CA (June 2012). "Pneumocystis jiroveci pneumonia: high-resolution CT findings in patients with and without HIV infection". AJR. American Journal of Roentgenology. 198 (6): W555–W561. doi:10.2214/AJR.11.7329. PMID 22623570. S2CID 7041746.
  8. ↑ Bennett NJ (2017-08-08). "What are possible complications of Pneumocystis jiroveci pneumonia (PJP)?". Medscape. Archived from the original on 2020-08-06. Retrieved 2023-01-29.
  9. ↑ Riedel S, Hobden JA, Miller S, Morse SA, Mietzner TA, Detrick B (2019). Jawetz, Melnick & Adelberg's Medical Microbiology (28th ed.). New York, NY. ISBN 9781260012026. OCLC 1101189928.
  10. ↑ Duboucher C, Boggia R, Morel G, Capron M, Pierce RJ, Dei-Cas E, Viscogliosi E (December 2007). "Pneumocystis pneumonia: immunosuppression, Pneumocystis jirovecii...and the third man". Nature Reviews. Microbiology. 5 (12): 967. doi:10.1038/nrmicro1621-c1. PMID 19507333. S2CID 33897311.
  11. ↑ Duboucher C (March 2021). "SARS-CoV-2 and superimposed infection by trichomonads". The Journal of Infection. 82 (3): e22–e23. doi:10.1016/j.jinf.2020.11.038. PMC 7834870. PMID 33271170.
  12. ↑ "Supplementary Information: Microscopic appearance of Pneumocystis jiroveci from bronchial washings". Archived from the original on 18 July 2009. Retrieved 5 June 2009.
  13. ↑ Medrano FJ, Montes-Cano M, Conde M, de la Horra C, Respaldiza N, Gasch A, et al. (February 2005). "Pneumocystis jirovecii in general population". Emerging Infectious Diseases. 11 (2): 245–250. doi:10.3201/eid1102.040487. PMC 3320436. PMID 15752442.
  14. ↑ Stern A, Green H, Paul M, Vidal L, Leibovici L (October 2014). "Prophylaxis for Pneumocystis pneumonia (PCP) in non-HIV immunocompromised patients". The Cochrane Database of Systematic Reviews. 10 (10): CD005590. doi:10.1002/14651858.CD005590.pub3. PMC 6457644. PMID 25269391.
  15. ↑ Ryan KJ, Ray CG, eds. (2004). Sherris Medical Microbiology (4th ed.). McGraw Hill. ISBN 978-0-8385-8529-0.
  16. ↑ Puzio J, Kucewicz E, Sioła M, Dworniczak A, Wojarski J, Zegleń S, et al. (2009). "[Atypical and opportunistic pulmonary infections after cardiac surgery]". Anestezjologia Intensywna Terapia (in polski). 41 (1): 41–45. PMID 19517677.
  17. 1 2 Morris A, Lundgren JD, Masur H, Walzer PD, Hanson DL, Frederick T, et al. (October 2004). "Current epidemiology of Pneumocystis pneumonia". Emerging Infectious Diseases. 10 (10): 1713–1720. doi:10.3201/eid1010.030985. PMC 3323247. PMID 15504255.
  18. ↑ Ponce CA, Gallo M, Bustamante R, Vargas SL (February 2010). "Pneumocystis colonization is highly prevalent in the autopsied lungs of the general population". Clinical Infectious Diseases. 50 (3): 347–353. doi:10.1086/649868. PMID 20047487.
  19. ↑ Schmoldt S, Schuhegger R, Wendler T, Huber I, Söllner H, Hogardt M, et al. (March 2008). "Molecular evidence of nosocomial Pneumocystis jirovecii transmission among 16 patients after kidney transplantation". Journal of Clinical Microbiology. 46 (3): 966–971. doi:10.1128/JCM.02016-07. PMC 2268360. PMID 18216217.
  20. ↑ Morris A, Beard CB, Huang L (January 2002). "Update on the epidemiology and transmission of Pneumocystis carinii". Microbes and Infection. 4 (1): 95–103. doi:10.1016/S1286-4579(01)01514-3. PMID 11825780.
  21. ↑ de Boer MG, Bruijnesteijn van Coppenraet LE, Gaasbeek A, Berger SP, Gelinck LB, van Houwelingen HC, et al. (May 2007). "An outbreak of Pneumocystis jiroveci pneumonia with 1 predominant genotype among renal transplant recipients: interhuman transmission or a common environmental source?". Clinical Infectious Diseases. 44 (9): 1143–1149. doi:10.1086/513198. PMID 17407029.
  22. ↑ Fannin S, Gottlieb MS, Weisman JD, et al. (1982). "A Cluster of Kaposi's Sarcoma and Pneumocystis carinii pneumonia among homosexual male residents of Los Angeles and Range Counties, California". MMWR Weekly. 31 (32): 305–7. Archived from the original on 2008-02-24. Retrieved 2023-01-29.
  23. ↑ Masur H, Michelis MA, Greene JB, Onorato I, Stouwe RA, Holzman RS, et al. (December 1981). "An outbreak of community-acquired Pneumocystis carinii pneumonia: initial manifestation of cellular immune dysfunction". The New England Journal of Medicine. 305 (24): 1431–1438. doi:10.1056/NEJM198112103052402. PMID 6975437.
  24. 1 2 Carmona EM, Limper AH (February 2011). "Update on the diagnosis and treatment of Pneumocystis pneumonia". Therapeutic Advances in Respiratory Disease. 5 (1): 41–59. doi:10.1177/1753465810380102. PMC 6886706. PMID 20736243.
  25. 1 2 Sternberg SD, Rosenthal JH (April 1955). "Interstitial plasma cell pneumonia". The Journal of Pediatrics. 46 (4): 380–393. doi:10.1016/S0022-3476(55)80142-4. PMID 14368443.
  26. 1 2 3 4 Elsevier, Dorland's Illustrated Medical Dictionary, Elsevier, archived from the original on 2014-01-11, retrieved 2023-01-29.
  27. ↑ Stringer JR, Beard CB, Miller RF, Wakefield AE (September 2002). "A new name (Pneumocystis jiroveci) for Pneumocystis from humans". Emerging Infectious Diseases. 8 (9): 891–896. doi:10.3201/eid0809.020096. PMC 2732539. PMID 12194762.
  28. ↑ Cushion MT (1998). "Ch. 34: Pneumocystis carinii". In Collier L, Balows A, Sussman M (eds.). Topley and Wilson's Microbiology and Microbial Infections (9th ed.). New York: Arnold and Oxford Press. pp. 645–683.
  29. ↑ Cushion MT (December 1998). "Taxonomy, genetic organization, and life cycle of Pneumocystis carinii". Seminars in Respiratory Infections. 13 (4): 304–312. PMID 9872627.
  30. ↑ Cushion MT (May 2004). "Pneumocystis: unraveling the cloak of obscurity". Trends in Microbiology. 12 (5): 243–249. doi:10.1016/j.tim.2004.03.005. PMID 15120144.
  31. ↑ Stringer JR, Beard CB, Miller RF, Wakefield AE (September 2002). "A new name (Pneumocystis jiroveci) for Pneumocystis from humans". Emerging Infectious Diseases. 8 (9): 891–896. doi:10.3201/eid0809.020096. PMC 2732539. PMID 12194762.
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