Monocytes loaded with indocyanine green as active homing contrast agents permit optical differentiation of infectious and non-infectious inflammation

Joani M. Christensen, Gabriel A. Brat, Kristine E. Johnson, Yongping Chen, Kate J. Buretta, Damon S. Cooney, Gerald Brandacher, W. P.Andrew Lee, Xingde Li, Justin M. Sacks

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Distinguishing cutaneous infection from sterile inflammation is a diagnostic challenge and currently relies upon subjective interpretation of clinical parameters, microbiological data, and nonspecific imaging. Assessing characteristic variations in leukocytic infiltration may provide more specific information. In this study, we demonstrate that homing of systemically administered monocytes tagged using indocyanine green (ICG), an FDA-approved near infrared dye, may be assessed non-invasively using clinically-applicable laser angiography systems to investigate cutaneous inflammatory processes. RAW 264.7 mouse monocytes co-incubated with ICG fluoresce brightly in the near infrared range. In vitro, the loaded cells retained the ability to chemotax toward monocyte chemotactic protein-1. Following intravascular injection of loaded cells into BALB/c mice with induced sterile inflammation (Complete Freund's Adjuvant inoculation) or infection (Group A Streptococcus inoculation) of the hind limb, noninvasive whole animal imaging revealed local fluorescence at the inoculation site. There was significantly higher fluorescence of the inoculation site in the infection model than in the inflammation model as early as 2 hours after injection (p<0.05). Microscopic examination of bacterial inoculation site tissue revealed points of near infrared fluorescence, suggesting the presence of ICG-loaded cells. Development of a non-invasive technique to rapidly image inflammatory states without radiation may lead to new tools to distinguish infectious conditions from sterile inflammatory conditions at the bedside.

Original languageEnglish (US)
Article numbere81430
JournalPloS one
Volume8
Issue number11
DOIs
StatePublished - Nov 25 2013
Externally publishedYes

Fingerprint

Indocyanine Green
monocytes
Contrast Media
Monocytes
inflammation
Fluorescence
fluorescence
Inflammation
Infrared radiation
Infection
image analysis
infection
injection
Imaging techniques
Skin
Injections
Angiography
Freund's Adjuvant
Chemokine CCL2
Streptococcus

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)
  • General

Cite this

Christensen, J. M., Brat, G. A., Johnson, K. E., Chen, Y., Buretta, K. J., Cooney, D. S., ... Sacks, J. M. (2013). Monocytes loaded with indocyanine green as active homing contrast agents permit optical differentiation of infectious and non-infectious inflammation. PloS one, 8(11), [e81430]. https://doi.org/10.1371/journal.pone.0081430

Monocytes loaded with indocyanine green as active homing contrast agents permit optical differentiation of infectious and non-infectious inflammation. / Christensen, Joani M.; Brat, Gabriel A.; Johnson, Kristine E.; Chen, Yongping; Buretta, Kate J.; Cooney, Damon S.; Brandacher, Gerald; Lee, W. P.Andrew; Li, Xingde; Sacks, Justin M.

In: PloS one, Vol. 8, No. 11, e81430, 25.11.2013.

Research output: Contribution to journalArticle

Christensen, JM, Brat, GA, Johnson, KE, Chen, Y, Buretta, KJ, Cooney, DS, Brandacher, G, Lee, WPA, Li, X & Sacks, JM 2013, 'Monocytes loaded with indocyanine green as active homing contrast agents permit optical differentiation of infectious and non-infectious inflammation', PloS one, vol. 8, no. 11, e81430. https://doi.org/10.1371/journal.pone.0081430
Christensen, Joani M. ; Brat, Gabriel A. ; Johnson, Kristine E. ; Chen, Yongping ; Buretta, Kate J. ; Cooney, Damon S. ; Brandacher, Gerald ; Lee, W. P.Andrew ; Li, Xingde ; Sacks, Justin M. / Monocytes loaded with indocyanine green as active homing contrast agents permit optical differentiation of infectious and non-infectious inflammation. In: PloS one. 2013 ; Vol. 8, No. 11.
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