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Cytomegalovirus

Cytomegalovirus (CMV), is a genus of Herpes viruses; in humans the species is known as Human herpesvirus 5 (HHV-5). It belongs to the Betaherpesvirinae subfamily of Herpesviridae. The name means "cell very big virus". more...

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CMV especially attacks salivary glands and may also be devastating or even fatal to fetuses. CMV infection can also be life threatening for patients who are immunocompromised (e.g. patients with HIV or organ transplant recipients). CMV viruses are found in many mammal species, but generally are specific only to that species.

Species

  • Cercopithecine herpesvirus 5 (CeHV-5) - African green monkey cytomegalovirus
  • Cercopithecine herpesvirus 8 (CeHV-8) - Rhesus monkey cytomegalovirus
  • Human herpesvirus 5 (HHV-5) - Human cytomegalovirus
  • Pongine herpesvirus 4 (PoHV-4)

Tentative species:

  • Aotine herpesvirus 1 (AoHV-1) - Herpesvirus aotus 1
  • Aotine herpesvirus 3 (AoHV-3) - Herpesvirus aotus 3

General information

Cytomegalovirus, or CMV, is found universally throughout all geographic locations and socioeconomic groups, and infects between 50% and 85% of adults in the United States by 40 years of age. CMV is also the virus most frequently transmitted to a developing child before birth. CMV infection is more widespread in developing countries and in areas of lower socioeconomic conditions. For most healthy persons who acquire CMV after birth there are few symptoms and no long-term health consequences. Some persons with symptoms experience infectious mononucleosis, with prolonged fever, and a mild hepatitis. A very sore throat is also common. Once a person becomes infected, the virus remains alive, but usually latent within that person's body for life. Recurrent disease rarely occurs unless the person's immune system is suppressed due to therapeutic drugs or disease. Therefore, for the vast majority of people, CMV infection is not a serious problem.

However, CMV infection is important to certain high-risk groups. Major areas of concern are (1) the risk of infection to the unborn baby during pregnancy, (2) the risk of infection to people who work with children, and (3) the risk of infection to the immunocompromised person, such as organ transplant recipients and persons infected with human immunodeficiency virus (HIV).

The virus acts by blocking cell apoptosis via the mitochondria and causing massive cell enlargement, which is the source of the virus' name.

Characteristics of the virus

CMV is a member of the herpesvirus group, which includes herpes simplex virus types 1 and 2, varicella-zoster virus (which causes chickenpox and shingles), and Epstein-Barr virus (which, together with CMV, is the main cause for infectious mononucleosis). These viruses share a characteristic ability to remain latent within the body over a long period.

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Immunity to CMV reduces risk of congenital infection - Tips from Other Journals - cytomegalovirus
From American Family Physician, 8/15/03 by Caroline Wellbery

Cytomegalovirus (CMV) can infect a fetus even if the mother has had remote infection before pregnancy. However, it is not known whether maternal CMV immunity reduces the risk of transplacental infection. Fowler and colleagues compared rates of congenital infection according to maternal serologic status before pregnancy.

The authors studied the records of 3,461 parturients who had at least one other delivery at the study hospital and whose previous offspring's cord serum specimens were available. Cord serum specimens from current and previous pregnancies were compared to determine seroconversion. Newborns were screened for congenital CMV infection.

At the time of the previous pregnancy, 2,857 (82.5 percent) of the mothers had CMV antibodies, and 604 (17.5 percent) were seronegative. Congenital CMV infection occurred in 46 infants (1.3 percent) of all the study mothers, with 18 (3 percent) occurring in seronegative mothers and 29 (1 percent) occurring in immune mothers. Of all the congenital CMV infections in the initially seronegative group, 142 mothers (23.5 percent) seroconverted between pregnancies.

Multivariate analysis, controlling for immune status at previous birth, age, race, insurance status, and gravidity, indicated that older maternal age (25 years or older) and maternal immunity were strongly associated with reduced risk of congenital CMV infection.

The authors conclude that young women who have immunity to CMV from naturally acquired infection are 69 percent less likely to give birth to an infant with congenital CMV infection than are those who are initially CMV seronegative. Risk for congenital CMV was particularly high in mothers who seroconverted in the average three-year interval between pregnancies.

This study provides an estimated CMV infection rate in the offspring of immune mothers of 1 percent. Remote immunity appears to have a protective effect, which suggests that a vaccine would reduce congenital CMV infection rates. In addition, because of the association between younger age and congenital CMV infection, postponing pregnancy until the woman is at least 20 years old could also reduce congenital CMV infection rates.

Caroline Wellbery, M.D.

Fowler KB, et al. Maternal immunity and prevention of congenital cytomegalovirus infection. JAMA February 26, 2003;289:1008-11.

COPYRIGHT 2003 American Academy of Family Physicians
COPYRIGHT 2003 Gale Group

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