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PERSPECTIVE | MPOX AND BREASTFEEDING
2025
:14;
e017
doi:
10.25259/IJMA_9_2025

Mpox and Breastfeeding in Sub-Saharan Africa: Clinical, Program, and Policy Recommendations

Department of Clinical Sciences, Higher Institute of Medical Technology Health Ebene Consulting, Yaounde, Cameroon.
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*Corresponding author: Anne Esther Njom Nlend, Department of Clinical Sciences, Higher Institute of Medical Technology Health Ebene Consulting, Yaounde, Cameroon. E-mail: anne.njom@gmail.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Njom Nlend A. Mpox and breastfeeding in subSaharan Africa: Clinical, program, and policy recommendations. Int J Matern Child Health AIDS. 2025;14:e017. doi: 10.25259/IJMA_9_2025

Abstract

This perspective paper explores the recommendations to maintain a secure breastfeeding in the case of the Mpox epidemic in lactating populations of sub-Saharan Africa. An emphasis is placed on prioritizing breastfeeding by own mother’s milk (OMM) through direct latching whenever possible. In case direct breastfeeding by OMM is impossible, clinicians and infant feeding counselors should promote expressed breast milk, pasteurized or not, and wet nursing. In all cases, policy makers and program managers will maintain the promotion of breastfeeding for the sake of infant survival.

Keywords

Breastfeeding
Mpox
Policy
Recommendations
Sub-Saharan Africa

INTRODUCTION

The monkeypox virus, also known as Mpox, is a deoxyribonucleic acid (DNA) virus belonging to the Orthopoxvirus family. It can provoke an acute infection after an incubation period ranging from 5 to 21 days (7 to 14 days on average). The clinical manifestations during the phase of invasion are similar to a pseudo-flu syndrome; other symptoms can be associated with vesiculo-pustular skin lesions. The mortality rate associated with this condition varies according to the classification assigned to it, which is based on 5 grades determined by the number of lesions per cm2, and according to the clade of the virus. Interhuman contamination is possible and occurs through skin lesions, respiratory droplets, biological fluids, and the sexual route.[1] Blood contamination is characterized by the brevity of viremia, which lasts about 2 days before the appearance of skin lesions. Vertical contamination would be possible either during pregnancy or after, during the postnatal period.[2,3] In utero infection can cause prematurity or stillbirths. It should be noted that perinatal mortality rates increase in the event of contamination, especially with Mpox Clade I.[3] Because of the particularity of the evolution of the monkeypox virus pandemic, it has been considered an epidemiological emergency with the imperative of implementing measures to secure the health of the mother and child. This document presents a point of view that aims to ensure the health of mothers and their newborns in areas where breastfeeding is essential to the survival of newborns and young infants. It addresses the following points: 1. The risk of transmission of the monkeypox virus during breastfeeding. 2. The timeframe of transmission of this virus. 3. The factors associated with a risk of transmission. 4. The ways of prevention. 5. The salient points to be considered for possible recommendations.

The Risk of Transmission of the Monkeypox Virus During Breastfeeding

According to data from the literature, the risk of viral infection with Mpox during breastfeeding is documented. Some case reports have described contamination from mother to child during breastfeeding by the horizontal route. In such case, contamination of the breastmilk is acquired through skin lesions expressed on the periphery of the mammary gland; in addition, vertical transmission is supported by the documented presence in breast milk of viruses found and authentication by polymerase chain reaction (PCR)-DNA virus detection techniques; According to the teams, the existence of a minimum concentration threshold is necessary to highlight the presence of the virus in breast milk.[4,5]

Factors Associated with Perinatal Transmission

Both the type of virus and the host can affect perinatal transmission. Epidemiological data report a greater severity and perinatal risk of Mpox Clade I, with a high lethality and poor outcomes recorded.[3] As for the host, several comorbidities affecting the immune capacity could explain more severe or more frequent forms. In addition, more severe cases have been recorded in newborns. Mpox should thus be added to the list of viruses and microorganisms that can be transmitted vertically from mother to child, such as human immunodeficiency virus, rubella, cytomegalovirus, herpes, and Toxoplasma.[6]

The Timing of Transmission of this Virus

The timing of viral transmission and the risk of infectivity could be correlated with the viral load, both perinatally and through breastfeeding. However, viral shedding could last throughout the eruption and could even precede it.[7] So far, any strategy of prevention should cover this time frame

What are the Possibilities for Prevention in an Epidemic Context

The goals are two-fold

First of all, prevent Mpox contamination in any breastfeeding woman, and second, put in place specific strategies for those infected for a safe practice of breastfeeding.

For all breastfeeding women

All contact with infected individuals should be avoided, and systematic prevention measures should be ensured by barrier methods. In the event of risky contact with an infected person, post-exposure prophylaxis can be offered to breastfeeding women by vaccination.[8]

In women infected with Mpox who are at risk of contamination

After diagnosis and screening for Mpox in breast milk by PCR/DNA and, if possible, culture, any assessment will be made on a case-by-case basis. The preferred option is to maintain breastfeeding in resource-limited regions of subSaharan Africa. This position opposes that of developed countries, which recommend stopping breastfeeding from the outset.[5] Furthermore, mother and co-rooming is to be prioritized to protect the early initiation and continuation of breastfeeding.[9]

In practice, all visible lesions and pustules on the breast will be covered. Hand hygiene, wearing a mask, and all barrier methods will be ensured before and after any contact, including breastfeeding and care of the baby. In case of unilateral skin lesions on the breast, the mother can extract and discard milk from the affected breast while continuing to breastfeed from the unaffected breast. In the event of bilateral lesions, breast milk can be extracted, pasteurized, and administered by cup. Pasteurization of breast milk can be both time-consuming and stigmatizing, which can make the procedure unsuccessful. Therefore, in case of failure of the previous process, infants aged <6 months and separated from their mother who has Mpox should be fed with donor human milk or appropriate breast milk substitutes (BMS), informed by feasibility, safety, sustainability, cultural context, acceptability to the mother, and service availability. BMS would be authorized in compliance with acceptable, feasible, affordable, sustainable and safe replacement feeding (AFASS) conditions (acceptable, the community does not stigmatize non breastfeeding mothers), feasible, (the mother must be committed to prepare the BMS at any time, affordable (the family should have proven capacity to buy the articifical milk at the indicated prices), sustainable (the BMS must be made available for at least 6 months) and safe (the environment must ensure safety around the prevention of diarrhea and infectious diseases and permanent access to potable water).[10,11] As a last resort, the possibility of breastfeeding by an uninfected wet nurse is possible. In all cases, monitoring of the mother, particularly of the newborn, will be carried out closely to ensure the absence of infection and contamination in the newborn or infant. Much remains unknown about the passage of the anti-Mpox antibody into breast milk. In addition, in the case of a mother undergoing antiviral treatment, few data are available regarding the passage of this product into breast milk and its possible role as a post-exposure prophylaxis therapy.[5]

CONCLUSION AND GLOBAL HEALTH IMPLICATIONS

Clinical data reveal the transmission of Mpox in women during breastfeeding by transcutaneous route from lesions around the areola or contamination after manual extraction of breast milk, and/or via breast milk. In the context of a monkeypox epidemic, for clinicians and infant feeding counsellors, breastfeeding will always be preferred, including the non-separation of the mother-child couple. This breastfeeding will be done directly by the mother or an uninfected wet nurse, using a healthy breast for latching. In other cases, administration of expressed and/or pasteurized breast milk will be supported. The usual anti-infectious precautions will be taken in the case of infected mothers: Covering the lesions, extraction, and throwing away milk from the infected nipple. The interruption of breastfeeding with the administration of BMS is the last measure, while ensuring the respect of AFASS conditions.

Program managers and policy makers should ensure the promotion of breastfeeding, as exclusive for the first 6 months of life and nonexclusive thereafter for 2 years, even beyond.

Key Messages

1. In lactating countries of Sub-Saharan Africa, the protection and safety of breastfeeding is an important key for infant survival in context of Mpox pandemic. 2. All stakeholders including, clinicians, program managers, and policy makers should maintain ongoing awareness of the benefit of breastfeeding as defined in infant feeding policy guidelines.

Acknowledgments:

None.

COMPLIANCE WITH ETHICAL STANDARDS

Conflicts of Interest: The author declares no competing interests. Financial Disclosure: Nothing to declare. Funding/Support: There was no funding for this study. Ethics Approval: Not applicable. Declaration of Patient Consent: Patient’s consent is not required, as there are no patients in this study. Use of Artificial Intelligence (AI)- Assisted Technology for Manuscript Preparation: The author confirms that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript, and no images were manipulated using AI. Disclaimer: None.

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