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Noninvasive PET Detection of CD69-Positive Immune Cells Before Signs of Clinical Disease in Inflammatory Arthritis.

Authors :
Puuvuori E
Shen Y
Hulsart-Billström G
Mitran B
Zhang B
Cheung P
Wegrzyniak O
Ingvast S
Persson J
Ståhl S
Korsgren O
Löfblom J
Wermeling F
Eriksson O
Source :
Journal of nuclear medicine : official publication, Society of Nuclear Medicine [J Nucl Med] 2024 Feb 01; Vol. 65 (2), pp. 294-299. Date of Electronic Publication: 2024 Feb 01.
Publication Year :
2024

Abstract

Rheumatoid arthritis (RA) is the most common inflammatory joint disease, and early diagnosis is key for effective disease management. CD69 is one of the earliest cell surface markers seen at the surface of activated immune cells, and CD69 is upregulated in synovial tissue in patients with active RA. In this study, we evaluated the performance of a CD69-targeting PET agent, [ <superscript>68</superscript> Ga]Ga-DOTA-Z <subscript>CAM241</subscript> , for early disease detection in a model of inflammatory arthritis. Methods: A model of inflammatory arthritis was induced by transferring splenocytes from KRN T-cell receptor transgenic B6 mice into T-cell-deficient I-A <superscript>g7</superscript> major histocompatibility complex class II-expressing recipient mice. The mice were examined longitudinally by [ <superscript>68</superscript> Ga]Ga-DOTA-Z <subscript>CAM241</subscript> PET/CT before and 3, 7, and 12 d after induction of arthritis. Disease progression was monitored by clinical parameters, including measuring body weight and scoring the swelling of the paws. The uptake of [ <superscript>68</superscript> Ga]Ga-DOTA-Z <subscript>CAM241</subscript> in the paws was analyzed and expressed as SUV <subscript>mean</subscript> Tissue biopsy samples were analyzed for CD69 expression by flow cytometry or immunostaining for a histologic correlate. A second group of mice was examined by a nonbinding, size-matched Affibody molecule as the control. Results: Clinical symptoms appeared 5-7 d after induction of arthritis. The uptake of [ <superscript>68</superscript> Ga]Ga-DOTA-Z <subscript>CAM241</subscript> in the joints was negligible at baseline but increased gradually after disease induction. An elevated PET signal was found on day 3, before the appearance of clinical symptoms. The uptake of [ <superscript>68</superscript> Ga]Ga-DOTA-Z <subscript>CAM241</subscript> correlated with the clinical score and disease severity. The presence of CD69-positive cells in the joints and lymph nodes was confirmed by flow cytometry and immunostaining. The uptake of the nonbinding tracer that was the negative control also increased gradually with disease progression, although to a lesser extent than with [ <superscript>68</superscript> Ga]Ga-DOTA-Z <subscript>CAM241</subscript> Conclusion: The uptake of [ <superscript>68</superscript> Ga]Ga-DOTA-Z <subscript>CAM241</subscript> in the inflamed joints preceded the clinical symptoms in the KRN T-cell transfer model of inflammatory arthritis, in accordance with immunostaining for CD69. [ <superscript>68</superscript> Ga]Ga-DOTA-Z <subscript>CAM241</subscript> is thus a promising PET imaging marker of activated immune cells in tissue during RA onset.<br /> (© 2024 by the Society of Nuclear Medicine and Molecular Imaging.)

Details

Language :
English
ISSN :
1535-5667
Volume :
65
Issue :
2
Database :
MEDLINE
Journal :
Journal of nuclear medicine : official publication, Society of Nuclear Medicine
Publication Type :
Academic Journal
Accession number :
38050119
Full Text :
https://doi.org/10.2967/jnumed.123.266336