Varicella-zoster virus (HHV-3) is a highly contagious virus that can cause either chickenpox or herpes zoster. It is transmitted mainly through inhalation of the virus-infected aerosolized droplets. It initially presents as an infection of the upper airway, which enters the circulation after 2 to 3 days. It subsequently causes another bout of viremia (after 10 to 12 days) when it presents with a characteristic, pruritic, vesicular rash over the skin and mucous membranes. Additional features include fever and a loss of appetite. This rash typically begins on the face and the trunk and then spreads to the extremities, usually resolving in 4 to 7 days. Individul=als produce immunoglobulins like IgA, IgM, IgG as a response to the infection, and IgG antibodies provide lifelong immunity against the virus. Varicella-Zoster Virus (VZV) can remain dormant in the sensory nerves after a primary varicella infection. Its reactivation can cause herpes zoster, a painful vesicular rash along a dermatome that does not cross the midline.[1]

VZV vaccinations, approved by the FDA, have significantly brought down the number of patients admitted with varicella each year in the United States. The vaccines are available for ages 12 months and older, making chickenpox a preventable disease. However, immunocompromised and pregnant patients are ineligible for these vaccinations.[2] 

Varicella-zoster immune globulin (VZIG) was first researched in the 1960s and prepared from patients recovering from varicella-zoster. It reduces the severity and attack rates of primary varicella. Following modification in the late 70s, the varicella immune globulin came onto the market for high-risk individuals with varicella exposure. It underwent further revision to the current immune globulin sold in the United States.

Varicella-zoster immune globulin should be a consideration for post-exposure prophylaxis in individuals who have a high risk of developing severe disease, who are lacking evidence of immunity, or who are ineligible for the vaccination.[3] The CDC recommends varicella-zoster immune globulin either immediately or up to 10 days following exposure for maximal efficacy for the following patient groups:

• Immunocompromised patients with no evidence of immunity (including those who have primary or secondary immunodeficiencies), patients who have an underlying neoplastic disease, and persons who are receiving immunosuppressive therapies - it is also indicated for patients undergoing hematopoietic cell transplantation who have not yet been re-immunized against varicella infection.
• Mothers of newborn infants who have signs and symptoms of varicella around the time of delivery (i.e., five days before delivery and up to two days after); VZV transmission can be transplacental (in utero) or can happen during a contact perinatally or postnatally.
• Premature infants hospitalized or born at ≥28 weeks of gestation whose mothers lack evidence of immunity to varicella.
• Premature infants hospitalized or born at <28 weeks of gestation or weighing <1000g at birth, even if their mothers have evidence of immunity to varicella.
• Pregnant women lacking evidence of immunity

Immunocompromised patients who were receiving a monthly high dose of intravenous immune globulin (IVIG) and received the dose <3 weeks before exposure, were likely to be protected from varicella.[3][4][5]

B lymphocytes (plasma cells) produce immunoglobulins, which function as antibodies and can recognize a vast spectrum of antigenic epitopes. Adequate functioning of these immunoglobulins is essential for a healthy humoral immune response. Each immunoglobulin structure is unique, and an extensive collection of immunoglobulins allows the body to respond to a wide variety of antigens.

The production of human immunoglobulin products is from an amalgamation of plasma from several donors; this ensures that the final product contains a wide variety of antibody repertoires with a collection of variable domains of antibodies within the regular serum. The IgG molecules must have suitable functional activities such as complement-mediated bactericidal activity, virus-neutralizing activity, opsonization (i.e., marking a pathogen for destruction), and the ability to inactivate toxins to create an effective immune response against a range of microorganisms.

The herpes zoster immune globulin contains antibodies (IgG) from pooled human plasma of individuals with high titers of varicella-zoster and therefore provides passive immunity.[6][7]

Human immunoglobulin products are available as intravenous immune globulin (IVIG), Subcutaneous immune globulin (SCIG), and intramuscular immune globulin (IMIG). Varicella-zoster immune globulin is available only as Intramuscular immune globulin (IMIG) in the United States. The FDA approved it in December 2012.

Varicella-zoster immune globulin comes in 125-IU vials, and administration should only be intramuscular and as directed by the manufacturer. No dose adjustments are recommended for renal or hepatic impairment. Individuals who later become eligible for vaccination should receive varicella vaccine ≥five months after varicella-zoster immune globulin administration.[3]

Local pain at the injection site is the most typical adverse reaction from medication administration. Statistically, a few (1 to 10%) patients have developed headaches, fatigue, and chills. Other less common reactions include skin rash and nausea. Very rarely, patients also develop DVT, serum sickness, hypersensitivity reaction, and thrombosis.[8]

Varicella-zoster immune globulin administration is contraindicated in patients with a history of IgA deficiency. Contraindications also include patients with a history of anaphylaxis to human immune globulin. Clinicians should not administer the drug once the clinical illness has developed as it is ineffective.[9][4]