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Table 2 Human studies investigating angiogenic and angiostatic parameters in patients with idiopathic interstitial pneumonias (1997–2003)

From: Angiogenesis in Interstitial Lung Diseases: a pathogenetic hallmark or a bystander?

Investigator (year)

Tissue samples Sample size

IIP

Studied Parameters

Summary

Limitations

Keane et al. 41(1997)

Lung specimens/50 patients/54 controls

IPF

CXCL8, 10

Increased levels of CXCL8,10 that favor angiogenesis

Incomplete analysis of the angiogenic network / In vivo micropocket assay

Lappi-Blanco et al.53 (1999)

Lung specimens/19 patients

IPF-COP

VWF, CD34+

 

Small sample size / Lack of knowledge regarding factors responsible for vascular heterogeneity

Meyer et al. 43 (2000)

BALF samples/32 patients/66 controls

IPF-CF-SARCO

VEGF

Decreased VEGF levels in IPF patients

Small number of patients / No correlation between serum and BALF levels / No correlation with clinical parameters of disease severity

Keane et al. 42 (2001)

Lung specimens/91 patients/78 controls

IPF

CXCL5

Increased CXCL5 levels in IPF patients

Incomplete analysis of the angiogenic network

Lappi-Blanco et al. 54(2002)

Lung specimens/19 patients

IPF-COP

VEGF, bFGF

Increased VEGF and bFGF levels in MB compared to FF

Small sample size / Lack of knowledge regarding angiostatic regulators

Koyama et al. 44 (2002)

BALF samples/49 patients/27controls

IPF-PF/CTD-SARCO

VEGF

Decreased VEGF levels in IPF patients

High variability between serum and BALF levels in health and disease

Renzoni et al. 45 (2003)

Lung specimens/17 patients/12 controls

CFA-SSc

Vascular density and distribution

Abnormal vascular distribution in areas proximal to gas exchange / Phenotypically altered vessels

Morphometric study not suitable to identify the role of angiogenesis in hypoxemia

  1. Abbreviations: BALF: Bronchoalveolar lavage fluid, bFGF: basic fibroblast growth factor, CF: Cystic fibrosis, CFA: Cryptogenic fibrosing alveolitis, COP: Cryptogenic organizing pneumonia, FF: Fibroblastic foci, IFN-γ: Interferon gamma, IIPs: Idiopathic Interstitial Pneumonias, IPF: Idiopathic pulmonary fibrosis, MB: Masson bodies, NSIP: Non-specific interstitial pneumonia, PF-CTD: Pulmonary fibrosis associated with a connective tissue disease, SARCO: Sarcoidosis, VEGF: Vascular endothelial growth factor