3,053
Views
1
CrossRef citations to date
0
Altmetric
Editorial

Interstitial Pneumonia with Autoimmune Features (IPAF): time to redefine the classification criteria

, &
Pages 131-133 | Received 06 Sep 2022, Accepted 04 Oct 2022, Published online: 11 Oct 2022

References

  • Fischer A, Antoniou KM, Brown KK, et al. An official European respiratory society/American thoracic society research statement: interstitial pneumonia with autoimmune features. Eur Respir J. 2015;46:976–987.
  • Mosca M, Tani C, Vagnani S, et al. The diagnosis and classification of undifferentiated connective tissue diseases. J Autoimmun. 2014;48-49:50–52.
  • Tan EM, Feltkamp TE, Smolen JS, et al. Range of antinuclear antibodies in “healthy” individuals. Arthritis Rheum. 1997;40:1601–1611.
  • Sambataro G, Sambataro D, Spicuzza L, et al. Progression and prognosis of Interstitial Pneumonia with Autoimmune Features (IPAF): a longitudinal, prospective, multi-centric study. Clin Exp Rheumatol. 2022. DOI:10.55563/clinexprheumatol/lycdca. in press.
  • Sambataro G, Vancheri A, Torrisi SE, et al. The morphological domain does not affect the rate of progression to defined autoimmune diseases in patients with interstitial pneumonia with autoimmune features. Chest. 2020;157:238–242. “UIPAF” patients showed a similar rate of progression towards ARDs compared with classic IPAF
  • Sebastiani M, Cassone G, De Pasquale L, et al. Interstitial pneumonia with autoimmune features: a single center prospective follow-up study. Autoimmun Rev. 2020;19:102451.
  • Cavagna L, Trallero-Araguas E, Meloni F, et al. Influence of antisynthetase antibodies specificities on antisynthetase syndrome clinical spectrum time course. J Clin Med. 2019;8:2013.
  • Sambataro G, Ferro F, Orlandi M, et al. Clinical, morphological features and prognostic factors associated with interstitial lung disease in primary Sjogren’s syndrome: a systematic review from the Italian Society of Rheumatology. Autoimmun Rev. 2020;19:102447.
  • Sambataro G, Ferrara CA, Spadaro C, et al. A new method for the assessment of myalgia in interstitial lung disease: association with positivity for myositis specific and myositis associated antibodies. Diagnostics (Basel). 2022;12:1139.
  • Sambataro G, Sambataro D, Torrisi SE, et al. Clinical, serological and radiological features of a prospective cohort of Interstitial Pneumonia with Autoimmune Features (IPAF) patients. Respir Med. 2019;150:154–160.
  • Johnson SR, Fransen J, Khanna D, et al. Validation of potential classification criteria for systemic sclerosis. Arthritis Care Res (Hoboken). 2012;64:358–367.
  • Chaurasia S, Haran A, Chawla P, et al. The clinical, radiological and laboratory profile of patients with interstitial pneumonitis with autoimmune features from India: an observational, cross-sectional study. Cureus. 2021;13:e15187.
  • Hazarika K, Sahoo RR, Mohindra N, et al. Clinical, radiologic and serologic profile of patients with interstitial pneumonia with autoimmune features: a cross-sectional study. Rheumatol Int. 2022;8:1431–1441. DOI: 10.1007/s00296-021-04883-7.
  • Lundberg IE, Tjarnlund A, Bottai M, et al. EULAR/ACR classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups. Ann Rheum Dis. 2017;76:1955–1964.
  • Infantino M, Palterer B, Biagiotti R, et al. Reflex testing of speckled cytoplasmic patterns observed in routine ANA Hep-2 indirect immunofluorescence with a multiplex anti-synthetase dot-blot assay: a multicentric pilot study. Immunol Res. 2018;66:74–78.
  • Baer AL, Mc Adams Demarco M, Shiboski SC, et al. The SSB-positive/SSA-negative antibody profile is not associated with key phenotypic features of sjogren’s syndrome. Ann Rheum Dis. 2015;74:1557–1561.
  • Chung JH, Cox CW, Montner SM, et al. CT features of the usual interstitial pneumonia pattern: differentiating connective tissue disease-associated interstitial lung disease from idiopathic pulmonary fibrosis. AJR Am J Roentgenol. 2018;210:307–313.
  • Sambataro G, Ferrara CA, Torrisi SE, et al. “Usual” interstitial pneumonia with autoimmune features: a prospective study on a cohort of idiopathic pulmonary fibrosis patients. Clin Exp Rheumatol. 2022;40:1324–1329.
  • Manfredi A, Sebastiani M, Cerri S, et al. Prevalence and Characterization of non-sicca onset primary Sjӧgren’s syndrome with interstitial lung involvement. Clin Rheumatol. 2017;36:1261–1268.
  • Sebastiani M, Triantafyllias K, Manfredi A, et al. Nailfold capillaroscopy characteristics of antisynthetase syndrome and possible clinical associations: results of a multicenter international study. J Rheumatol. 2019;46:279–284.
  • Sambataro D, Sambataro G, Libra A, et al. Nailfold videocapillaroscopy is a useful tool to recognize definite forms of systemic sclerosis and idiopathic inflammatory myositis in interstitial lung disease patients. Diagnostics (Basel). 2020;10:253.
  • Zanframundo G, Faghili-Kashani S, Scirè CA, et al. Defining anti-synthetase syndrome: a systematic literature review. Clin Exp Rheumatol. 2022;40:309–319.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.