Serological And Cytokine Profiling of Umbilical Cord Blood for Maternal Torch Infections: A Cross-Sectional Study on Neonatal Risk in Yaoundé, Cameroon
DOI:
https://doi.org/10.14738/bjhr.1303.1277Keywords:
umbilical cord blood, TORCH infections, cytokine profiling, neonatal immunity, vertical transmission, Cameroon, sub-Saharan Africa, congenital infectionsAbstract
Background: Umbilical cord blood (UCB) represents a valuable biological matrix for assessing neonatal exposure to maternal infections and immune status at birth. In resource-limited settings such as Cameroon, its diagnostic potential remains underutilized, particularly for the detection of vertically transmitted infections within the TORCH complex ˗ Toxoplasma gondii, Rubella virus (Rubivirus rubellae), Cytomegalovirus (CMV)/ Human Herpesvirus 5 (HHV-5), and Herpes Simplex Virus types 1 and 2 (HSV-1/2). Objectives: This study aimed to determine the seroprevalence of TORCH infections in maternal venous blood and UCB, and to compare cytokine profiles in order to characterize neonatal immune activation at birth. Methods: A cross-sectional study was conducted from June to December 2024 across two referral hospitals in Yaoundé, Cameroon. A total of 108 mother-newborn pairs were enrolled consecutively. Paired maternal venous blood and UCB samples were tested using EVANCARE IgM/IgG TORCH rapid diagnostic tests (RDT), and ELISA-based ProcartaPlex™ multiplex cytokine profiling (12 analytes). Results: TORCH seroprevalence in UCB reflected maternal infection status, with high concordance for Toxoplasma gondii (90.0%; maternal 77.5% vs. UCB 72.5%) and CMV (70.0%; maternal 55.0% vs. UCB 50.0%). Cytokine profiling revealed that 10 of 12 analytes differed between compartments; IL-6 was significantly higher in maternal plasma (33.94 vs. 25.01 pg/mL; p < 0.0001) while IL-2 was significantly elevated in UCB (17.43 vs. 16.54 pg/mL; p = 0.04), with IL-4 and IL-5 showing identical values across both compartments. Conclusion: Maternal TORCH infections exert a measurable burden on neonatal infectious and immunological status at birth. UCB represents a non-invasive and ethically advantageous specimen for neonatal assessment. These findings support the integration of TORCH screening and UCB cytokine analysis into routine antenatal care protocols in low-resource settings to reduce neonatal morbidity.
References
Lawn JE, Cousens S, Zupan J. 4 million neonatal deaths: When? Where? Why? Lancet.
Neu N, Duchon J, Zachariah P. TORCH infections. Clin Perinatol. 2015;42(1):77–103.
Coyne CB, Lazear HM. Zika virus—reigniting the TORCH. Nat Rev Microbiol. 2016;14(11):707–715.
Hellström W, Forssell L, Morsing E, Sävman K, Ley D. Neonatal clinical blood sampling led to major blood loss and was associated with bronchopulmonary dysplasia. Acta Paediatr.
Aboalqez A, Deindl P, Ebenebe CU, Singer D, Blohm ME. Iatrogenic blood loss in very low birth weight infants and transfusion of packed red blood cells in a tertiary care neonatal intensive care unit. Children. 2021;8(10):847.
Delneste Y, Beauvillain C, Jeannin P. Innate immunity: structure and function of TLRs. Med Sci (Paris). 2007;23(1):67–73.
Burl S, Townend J, Njie-jobe J, et al. Age-dependent maturation of Toll-like receptormediated cytokine responses in Gambian infants. PLoS ONE. 2011;6(4):e18185.
Martin PL, Kurtzberg J, Hesse B. Umbilical cord blood: a guide for primary care physicians. Am Fam Physician. 2011;84(6):661–666. Scholar Publishing
Evancare Medical. High Accuracy Rapid Combo IgG/IgM TORCH Test Kits [package insert]. Nantong, Jiangsu Province, China: Evancare Medical; 2020.
Thermo Fisher Scientific. ProcartaPlex™ Human Simplex and Combinable Panels User Guide (MAN0028348). Waltham, MA: Thermo Fisher Scientific; 2024.
International Organization for Standardization. ISO 15189:2022 — Medical Laboratories: Requirements for Quality and Competence. Geneva: ISO; 2022.
Olarewaju O, Blumberg L, Mahomed K, Girdler-Brown B. Seroprevalence of TORCH infections in pregnant women attending antenatal care in Pretoria. S Afr Med J. 2016;106(4):378–382.
Sake CS, Eteme Enama S, Koga Mang’Dobara, Taidjague Dayang Ela, Nkadji Vignie Amora, Limane Adjobma Basile, Njiki Bikoi AU, Njiki-Bikoi J. Seroprevalence of anti-TORCH IgG/IgM (Toxoplasma gondii, Rubella sp, Cytomegalovirus, Herpes simplex virus 1/2) and associated risk factors in pregnant women in Yaoundé. ISAR J Med Pharm Sci. 2024;2(6):1–9.
Pappas G, Roussos N, Falagas ME. Toxoplasmosis snapshots: global status of Toxoplasma gondii seroprevalence and implications for pregnancy and congenital toxoplasmosis. Int J Parasitol. 2009;39(12):1385–1394.
Palmeira P, Quinello C, Silveira-Lessa AL, Zago CA, Carneiro-Sampaio M. IgG placental transfer in healthy and pathological pregnancies. Clin Dev Immunol. 2012;2012:985646.
Eno AA, Makemgue LS, Tonye DS III, Boye CSB, Seck A, Bercion R, Vauloup Fellous C, Tchuem Tchuente LA. Seroprevalence of rubella-specific IgM and IgG antibodies among pregnant women in a Catholic Hospital in Yaoundé, Cameroon. Int J Biol Chem Sci. 2018;12(3):1123–1130.
Gomez R, Romero R, Edwin SS, David C. Pathogenesis of preterm labor and preterm premature rupture of membranes associated with intraamniotic infection. Infect Dis Clin North Am. 1997;11(1):135–176.
Burl S, Townend J, Njie-Jobe J, et al. Age-dependent maturation of cytokine responses in neonates: implications for innate immune activation. J Infect Dis. 2011;204(3):460–469.
Hunter CA, Jones SA. IL-6 as a keystone cytokine in health and disease. Nat Immunol.
Malek TR. The biology of interleukin-2. Annu Rev Immunol. 2008;26:453–479.
Adkins B, Leclerc C, Marshall-Clarke S. Neonatal adaptive immunity comes of age. Nat Rev Immunol. 2004;4(7):553–564.
Burt TD. Fetal regulatory T cells and peripheral immune tolerance in utero: implications for development and disease. Am J Reprod Immunol. 2013;69(4):346–358.
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