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Increased Uptake of 111In-Octreotide in Idiopathic Pulmonary Fibrosis

Rachida Lebtahi1–5,, Severine Moreau2, Sylvain Marchand-Adam2–4,, Marie-Pierre Debray3, Michel Brauner6, Paul Soler4, Joëlle Marchal4, Olivier Raguin5, Anne Gruaz-Guyon5, Jean-Claude Reubi7, Dominique Le Guludec1–5, and Bruno Crestani2–4,

1 Department of Nuclear Medicine, Hôpital Bichat, Assistance Publique-Hôpitaux de Paris, Paris, France; 2 Department of Pneumology, Hôpital Bichat, Assistance Publique-Hôpitaux de Paris, Paris, France; 3 Department of Radiology, Hôpital Bichat, Assistance Publique-Hôpitaux de Paris, Paris, France; 4 INSERM Unit 700, Faculté Xavier Bichat, Université Paris 7 Denis Diderot, Paris, France; 5 EA 3512, Faculté Xavier Bichat, Université Paris 7 Denis Diderot, Paris, France; 6 Department of Radiology, Hôpital Avicenne, Assistance Publique Hôpitaux de Paris, Université Paris 13, Paris, France; and 7 Division of Cell Biology and Experimental Cancer Research, Institute of Pathology, University of Berne, Berne, Switzerland


Figure 1
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FIGURE 1.  Octreotide scintigraphy. (A) In patient with carcinoid tumor of digestive tract without lung involvement, no octreotide uptake is seen in lung. (B–E) In 2 patients with IPF, diffuse uptake of 111In-octreotide is seen in both lungs, but extent of CT abnormalities differs (L/B of 2.82 and 2.63 and total CT score of 2.8 and 3 for patient in B and D and patient in C and E, respectively).

 

Figure 2
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FIGURE 2.  Autoradiography from fibrotic lung sample, with enlarged views of boxed areas shown on right. (A) Hematoxylin- and eosin-stained section showing blood vessels (arrowheads). (B) Autoradiogram showing total binding of [125I-Tyr3]octreotide. Medium-sized vessels are clearly labeled (arrowheads). Weak labeling may also be seen in some lymphoid aggregates. (C) Autoradiogram showing strong, nonspecific binding that remains in presence of octreotide (1 µmol/L) in several elements of lung. Bar = 1 mm.

 

Figure 3
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FIGURE 3.  Inhibition of [125I-Tyr11]somatostatin-14 binding to cultured lung fibroblasts from IPF and control patients by somatostatin-14 and octreotide. Fibroblasts were incubated for 1 h at 37°C with [125I-Tyr11]somatostatin-14 alone (0.2 nmol/L, white bars) or in presence of somatostatin-14 (10–6 mol/L, hatched bars) or octreotide (10–6 mol/L, black bars). For each patient, results are expressed as mean ± SEM of 4–6 determinations of bound disintegrations per minute (dpm) normalized to 106 cells. *P < 0.05 vs. [125I-Tyr11]somatostatin alone. **P < 0.01 vs. [125I-Tyr11]somatostatin alone.

 





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