The spinal cord injury-induced immune deficiency syndrome: results of the SCIentinel study

• Published in: Brain (London, England : 1878) England : 1878), 2023-08, Vol.146 (8), p.3500-3512
• Main Authors: Kopp, Marcel A, Meisel, Christian, Liebscher, Thomas, Watzlawick, Ralf, Cinelli, Paolo, Schweizerhof, Oliver, Blex, Christian, Lübstorf, Tom, Prilipp, Erik, Niedeggen, Andreas, Druschel, Claudia, Schaser, Klaus-Dieter, Wanner, Guido A, Curt, Armin, Lindemann, Gertraut, Nugeva, Natalia, Fehlings, Michael G, Vajkoczy, Peter, Cabraja, Mario, Dengler, Julius, Ertel, Wolfgang, Ekkernkamp, Axel, Rehahn, Kerstin, Martus, Peter, Volk, Hans-Dieter, Unterwalder, Nadine, Kölsch, Uwe, Brommer, Benedikt, Hellmann, Rick C, Baumgartner, Elias, Hirt, Julian, Geurtz, Laura-Christin, Saidy, Ramin Raul Ossami, Prüss, Harald, Laginha, Ines, Failli, Vieri, Grittner, Ulrike, Dirnagl, Ulrich, Schwab, Jan M
• Format: Article
• Language: English
• Subjects: Cohort Studies; HLA-DR Antigens; Humans; Monocytes; Original; Prospective Studies; Spinal Cord Injuries - complications; Syndrome
• ISSN: 0006-8950; 1460-2156
• DOI: 10.1093/brain/awad092

Abstract Infections are prevalent after spinal cord injury (SCI), constitute the main cause of death and are a rehabilitation confounder associated with impaired recovery. We hypothesize that SCI causes an acquired lesion-dependent (neurogenic) immune suppression as an underlying mechanism to facilitate infections. The international prospective multicentre cohort study (SCIentinel; protocol registration DRKS00000122; n = 111 patients) was designed to distinguish neurogenic from general trauma-related effects on the immune system. Therefore, SCI patient groups differing by neurological level, i.e. high SCI [thoracic (Th)4 or higher]; low SCI (Th5 or lower) and severity (complete SCI; incomplete SCI), were compared with a reference group of vertebral fracture (VF) patients without SCI. The primary outcome was quantitative monocytic Human Leukocyte Antigen-DR expression (mHLA-DR, synonym MHC II), a validated marker for immune suppression in critically ill patients associated with infection susceptibility. mHLA-DR was assessed from Day 1 to 10 weeks after injury by applying standardized flow cytometry procedures. Secondary outcomes were leucocyte subpopulation counts, serum immunoglobulin levels and clinically defined infections. Linear mixed models with multiple imputation were applied to evaluate group differences of logarithmic-transformed parameters. Mean quantitative mHLA-DR [ln (antibodies/cell)] levels at the primary end point 84 h after injury indicated an immune suppressive state below the normative values of 9.62 in all groups, which further differed in its dimension by neurological level: high SCI [8.95 (98.3% confidence interval, CI: 8.63; 9.26), n = 41], low SCI [9.05 (98.3% CI: 8.73; 9.36), n = 29], and VF without SCI [9.25 (98.3% CI: 8.97; 9.53), n = 41, P = 0.003]. Post hoc analysis accounting for SCI severity revealed the strongest mHLA-DR decrease [8.79 (95% CI: 8.50; 9.08)] in the complete, high SCI group, further demonstrating delayed mHLA-DR recovery [9.08 (95% CI: 8.82; 9.38)] and showing a difference from the VF controls of −0.43 (95% CI: −0.66; −0.20) at 14 days. Complete, high SCI patients also revealed constantly lower serum immunoglobulin G [−0.27 (95% CI: −0.45; −0.10)] and immunoglobulin A [−0.25 (95% CI: −0.49; −0.01)] levels [ln (g/l × 1000)] up to 10 weeks after injury. Low mHLA-DR levels in the range of borderline immunoparalysis (below 9.21) were positively associated with the occurrence and earlier onset of infections, which