CC BY-NC-ND 4.0 · J Lab Physicians 2023; 15(02): 264-268
DOI: 10.1055/s-0042-1757720
Original Article

Salivary IgA as a Surrogate Biomarker for Microbial Infections in Postoperative Patients Receiving Chemo-Radio-Therapy for Head and Neck Cancer

Preeti Chavan
1   Composite Laboratory, Advanced Centre for Treatment, Research and Education in Cancer-Tata Memorial Centre, Homi Bhabha National Institute, Navi Mumbai, Maharashtra, India
,
2   Department of Microbiology, Advanced Centre for Treatment, Research and Education in Cancer-Tata Memorial Centre, Homi Bhabha National Institute, Navi Mumbai, Maharashtra, India
,
Amit Joshi
3   Department of Medical Oncology, Advanced Centre for Treatment, Research and Education in Cancer-Tata Memorial Centre, Homi Bhabha National Institute, Navi Mumbai, Maharashtra, India
,
Tejpal Gupta
4   Department of Radiation Oncology, Advanced Centre for Treatment, Research and Education in Cancer-Tata Memorial Centre, Homi Bhabha National Institute, Navi Mumbai, Maharashtra. India
,
Vedang Murthy
4   Department of Radiation Oncology, Advanced Centre for Treatment, Research and Education in Cancer-Tata Memorial Centre, Homi Bhabha National Institute, Navi Mumbai, Maharashtra. India
,
Vanita Noronha
3   Department of Medical Oncology, Advanced Centre for Treatment, Research and Education in Cancer-Tata Memorial Centre, Homi Bhabha National Institute, Navi Mumbai, Maharashtra, India
,
Divya Rathish
2   Department of Microbiology, Advanced Centre for Treatment, Research and Education in Cancer-Tata Memorial Centre, Homi Bhabha National Institute, Navi Mumbai, Maharashtra, India
,
Kumar Prabhash
3   Department of Medical Oncology, Advanced Centre for Treatment, Research and Education in Cancer-Tata Memorial Centre, Homi Bhabha National Institute, Navi Mumbai, Maharashtra, India
› Author Affiliations
Funding This study was funded by the Tata Memorial Centre through intramural funds.

Abstract

Objective Radiotherapy (RT) and chemotherapy (CT) are important treatment options in patients with head and neck cancers. A common complication of this is microbial colonization or infection of mucosal surfaces. These infections may commonly be due to bacteria or yeasts. Salivary proteins with their buffering activity and immunoglobulin, especially immunoglobulin A (IgA), protect oral tissue, mucosal surfaces, and teeth from various microorganisms. This study characterizes the common microorganisms encountered and evaluates the role of salivary IgA in predicting microbial infections in this group of patients with mucositis.

Methods A total of 150 adult head and neck cancer patients on CTRT were evaluated at baseline and at the end of 3 and 6 weeks, respectively. Oral swabs collected from buccal mucosa were processed in the microbiology laboratory for the presence of microorganisms. Saliva was processed for IgA level estimation on Siemens Dimension Automated biochemistry analyzer.

ResultsPseudomonas aeruginosa and Klebsiella pneumoniae were the most common organisms found in our patients, followed by Escherichia coli and group A beta-hemolytic Streptococci. A significant increase (p = 0.0203) in the incidence of bacterial infection was observed in post-CTRT patients (61%) compared to pre-CTRT patients (49.33%). There was significant increase in levels of salivary IgA (p = 0.003) in patients with bacterial and fungal infection (n = 135/267) when compared to those in samples showing no growth (n = 66/183).

Conclusion A significant increase in the incidence of bacterial infection in post-CTRT patients was observed in this study. This study also indicated that postoperative head and neck cancer patients with oral mucositis that developed an infection were associated with high salivary IgA levels, and it may serve as a surrogate biomarker of infection in these patients.

Note

Part of this study was presented at the 70th AACC annual scientific meeting and clinical lab expo organized in Chicago in 2018 as a poster.


Authors' Contributions

P.D.C., V.G.B., and A.J. researched literature and conceived the study. P.D.C., V.G.B., A.J., T.G., V.M., V.N., R.D., and K.P. were involved in protocol development, gaining ethical approval, and patient recruitment. P.D.C. and V.G.B. did data analysis. P.D.C. wrote the first draft of the manuscript. All authors reviewed and edited the manuscript and approved the final version of the manuscript.


Ethical Approval

This study was approved by Institutional Ethics Committee (ref no: project no 134, TMC-ACTREC IEC).




Publication History

Article published online:
30 January 2023

© 2023. The Indian Association of Laboratory Physicians. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Rodríguez-Caballero A, Torres-Lagares D, Robles-García M, Pachón-Ibáñez J, González-Padilla D, Gutiérrez-Pérez JL. Cancer treatment-induced oral mucositis: a critical review. Int J Oral Maxillofac Implants 2012; 41 (02) 225-238
  • 2 Ruescher TJ, Sodeifi A, Scrivani SJ, Kaban LB, Sonis ST. The impact of mucositis on alpha-hemolytic streptococcal infection in patients undergoing autologous bone marrow transplantation for hematologic malignancies. Cancer 1998; 82 (11) 2275-2281
  • 3 Bensadoun RJ, Patton LL, Lalla RV, Epstein JB. Oropharyngeal candidiasis in head and neck cancer patients treated with radiation: update 2011. Support Care Cancer 2011; 19 (06) 737-744
  • 4 de Barros Pontes C, Polizello ACM, Spadaro ACC. Clinical and biochemical evaluation of the saliva of patients with xerostomia induced by radiotherapy. Braz Oral Res 2004; 18 (01) 69-74
  • 5 Chiappin S, Antonelli G, Gatti R, De Palo EF. Saliva specimen: a new laboratory tool for diagnostic and basic investigation. Clin Chim Acta 2007; 383 (1-2): 30-40
  • 6 Silverman Jr S, Luangjarmekorn L, Greenspan D. Occurrence of oral Candida in irradiated head and neck cancer patients. J Oral Med 1984; 39 (04) 194-196
  • 7 Raj S, Sharma D, Mate P, Capoor MR, Bhowmik KT. A study of changes in the oral fungal flora of patients on radiotherapy for head and neck malignancies and their correlation with funguria and fungemia. Indian J Cancer 2017; 54 (01) 39-42
  • 8 Panghal M, Kaushal V, Kadayan S, Yadav JP. Incidence and risk factors for infection in oral cancer patients undergoing different treatments protocols. BMC Oral Health 2012; 12: 22
  • 9 Malamud D, Abrams WR, Barber CA, Weissman D, Rehtanz M, Golub E. Antiviral activities in human saliva. Adv Dent Res 2011; 23 (01) 34-37
  • 10 Malamud D. Saliva as a diagnostic fluid. Dent Clin North Am 2011; 55 (01) 159-178
  • 11 Nogueira RD, Sesso ML, Borges MC, Mattos-Graner RO, Smith DJ, Ferriani VP. Salivary IgA antibody responses to Streptococcus mitis and Streptococcus mutans in preterm and fullterm newborn children. Arch Oral Biol 2012; 57 (06) 647-653
  • 12 Pedersen SS, Møller H, Espersen F, Sørensen CH, Jensen T, Høiby N. Mucosal immunity to Pseudomonas aeruginosa alginate in cystic fibrosis. Acta Pathol Microbiol Scand Suppl 1992; 100 (04) 326-334
  • 13 Smith DJ, King WF, Taubman MA. Salivary IgA antibody to oral streptococcal antigens in predentate infants. Oral Microbiol Immunol 1990; 5 (02) 57-62
  • 14 Aanaes K, Johansen HK, Poulsen SS, Pressler T, Buchwald C, Høiby N. Secretory IgA as a diagnostic tool for Pseudomonas aeruginosa respiratory colonization. J Cyst Fibros 2013; 12 (01) 81-87
  • 15 Maurer MA, Meyer L, Bianchi M. et al. Glycosylation of human IgA directly inhibits influenza A and other sialic-acid-binding viruses. Cell Rep 2018; 23 (01) 90-99