Subcutaneous immunoglobulin therapy: a new option for patients with primary immunodeficiency diseases

Abstract

Since the 1950s, replacement of immunoglobulin G using human immunoglobulin has been the standard treatment for primary immunodeficiency diseases with defects in antibody production. These patients suffer from recurrent and severe infections, which cause lung damage and shorten their life span. Immunoglobulins given intravenously (IVIG) every 3–4 weeks are effective in preventing serious bacterial infections and improving the quality of life for treated patients. Administration of immunoglobulin subcutaneously (SCIG) is equally effective in preventing infections and has a lower incidence of serious adverse effects compared to IVIG. The tolerability and acceptability of SCIG has been demonstrated in numerous studies showing improvements in quality of life and a preference for subcutaneous immunoglobulin therapy in patients with antibody deficiencies.

Background

Primary immunodeficiency diseases (PIDD) are a group of over 150 disorders due to defects in critical pathways involved in host defense against infection and immune regulation. PIDD are due to single-gene defects, the causative mutation having been identified in more than 140 of these disorders. The underlying immune defect can impair innate immunity or adaptive immunity, but all patients with PIDD have an increased susceptibility to infection. More than 50% of PIDD are due to defects in antibody production (Table 1).¹ In addition to recurrent and severe bacterial infections, patients with antibody deficiencies also have an increased frequency of autoimmune disease, inflammatory disorders, and lymphoproliferative disorders. Life expectancy is reduced and recurrent infections cause significant morbidity and disability due to complications from chronic lung disease, inflammatory bowel disease and autoimmune disorders.

Table 1.

Primary immunodeficiencies: antibody deficiencies

Disorder	Gene (if known)	IgG replacement indicated?
Agammaglobulinemia
X-linked agammaglobulinemia	Btk	Yes
μ heavy chain deficiency	IGHM	Yes
Igα deficiency	CD79A	Yes
Igβ deficiency	CD79B	Yes
B-cell linker protein	BLNK	Yes
Common variable immune deficiency
Immune co-stimulator protein	ICOS	Yes
CD19 deficiency	CD19	Yes
CD20 deficiency	CD20	Yes
TACI deficiency	TNFRSF13B	Yes
BAFF receptor deficiency	TNFRSF13C	Yes
CVID	Unknown	Yes
Other antibody deficiencies
Selective IgA deficiency	Unknown	No
IgG subclass deficiency	Unknown	If recurrent infections
Specific antibody deficiency	Unknown
Transient hypogammaglobulinemia of infancy	Unknown
Other PIDD with antibody deficiency
HyperIgM syndrome X-linked	CD40L	Yes
Autosomal recessive	AID, UNG	Yes
Severe combined immune deficiency	Various	Yes
Wiskott–Aldrich syndrome	WASP	Yes
Ataxia-telangiectasia syndrome	ATM	Yes
Reticular dysgenesis	AK2	Yes
DiGeorge syndrome	22q11.2/10p13 deletion	Only for patients with low IgG

Note: Data based on IUIS classification of primary immune deficiencies.¹

Abbreviations: IgG, immunoglobulin G; Btk, Bruton’s tyrosine kinase; TACI, transmembrane activator and calcium-modulating cyclophilin ligand interactor; TNFRSF, tumor necrosis factor receptor super family; BAFF, B-cell activating factor; CVID, common variable immune deficiency; CD40L, CD40 ligand; AID, activating inducing cytidine deaminase; UNG, uracil DNA glycosylase; WASP, Wiskott–Aldrich syndrome protein; ATM, ataxia-telangiectasia mutated; AK2, adenylate kinase 2.

Since the 1950s, replacement of serum immunoglobulin G (IgG) with human immune globulin products has been the standard of treatment for patients with hypo/agammaglobulinemia and a significant impairment of specific antibody formation.² The first human immunoglobulin (IG) products were administered intramuscularly and were effective in decreasing mortality. However, it was difficult to maintain physiologically normal levels of serum IgG due to limitations in the dose of IG that could be administered. Intramuscular injections were painful and early IG products contained aggregates of IgG that caused serious adverse effects. Slow subcutaneous infusions of IG (SCIG) were used in the early 1980s to treat antibody deficiency, but the acceptance of this therapy was limited by the length of time for infusion and the volumes that could be infused.^3–6 In the 1980s, the development of IgG products for intravenous administration (IVIG) that contained only monomers of IgG, allowed patients to receive sufficient quantities of IgG to achieve serum levels in the physiologic range with fewer side effects. These products could be given monthly, and with higher levels of IgG, further decreased morbidity from infection and increased survival, as well as overall quality of life.

In 1991, Gardulf et al reported the use of infusion pumps to administer SCIG as a rapid infusion.⁷ For the past two decades, SCIG has been the treatment of choice for patients with antibody deficiencies in Sweden, while IVIG has been the standard treatment in the United States (US). Since 2006, when the United States Food and Drug Administration (FDA) approved the first SCIG, the use of SCIG to treat patients with PIDD and antibody deficiency has been steadily increasing.⁸ SCIG has been demonstrated to be effective and safe and has important advantages of tolerability, ease of administration and quality of life (QOL) improvements over IVIG. The development of higher concentration IgG products, improved delivery devices, and alternate methods of delivery will further increase the use of SCIG for the treatment of PIDD with antibody deficiency.

Immune globulin preparation

IG products used for intravenous (IV) or subcutaneous (SC) administration are collected from human donors at plasma collection centers. The pooled plasma from more than 5000 donors is treated using modified Cohn-Oncley cold ethanol fractionation, which separates the plasma into IgG, albumin, and clotting factors. Plasma donors are screened for high risk behaviors and the plasma fractions are tested for Hepatitis B surface antigen, HIV-1/HIV-2 antibodies, and Hepatitis C virus (HCV) antibody. Most products also test plasma pools using HIV-1 and HCV nucleic acid testing. After Cohn fractionation, the IgG may be further purified using anion exchange chromatography and (in some products) caprylate precipitation. The immunoglobulin plasma pool undergoes additional viral inactivation steps such as heat treatment, enzyme treatment, solvent/detergent treatment, low pH incubation, and/or nanofiltration. These steps have been shown to reduce the viral load for enveloped viruses (eg, HIV, West Nile virus, Hepatitis C virus) by 10¹² to 10¹⁶, nonenveloped viruses (eg, Hepatitis A virus, parvovirus) by 10⁵ to 10¹⁰, and prions (Creuzfeldt–Jakob).^9–15

Despite differences in viral inactivation steps and the use of different agents as stabilizing or buffering agents, all IG products contain 97%–98% IgG monomers with trace amounts of IgM, as well as IgG specific antibodies against a broad spectrum of bacterial and viral pathogens. IG products approved for SC administration contain varying concentrations of IgA (37–50 mcg/mL).^9,11,12 Currently available preparations of IVIG are available as 5% (5 g/100 mL) or 10% (10 g/100 mL) solutions.^9–11 Some are lyophilized and need to be reconstituted before administration, but the majority of products are available as liquid (ready to use) preparations. Three of the products approved by the FDA for SC administration in PIDD (all 10% IG) also have approval for IV administration. One SCIG product approved solely for SC administration (20% IG) is manufactured using the same process as the IVIG products. Table 2 describes the characteristics of IG products approved by the FDA for SC administration.

Table 2.

Subcutaneous immune globulin preparations (US) – properties and characteristics

Product	IgG concentration	IgA content	Stabilizer	Viral inactivation
Gammagard liquid	100 mg/mL	37 mcg/mL	Glycine	Solvent/detergent Nanofiltration Low pH/temperature
Gammaked™	100 mg/mL	46 mcg/mL	Glycine	Low pH Caprylate precipitation Depth filtration
Gamunex-C	100 mg/mL	46 mcg/mL	Glycine	Low pH Caprylate precipitation Depth filtration
Hizentra®	200 mg/mL	<50 mcg/mL	L-proline	Low pH Nanofiltration Depth filtration

Note: Data drawn from package inserts.⁹–¹²

Pharmacokinetics

During SC administration the IgG product is infused into the SC space. After receiving IVIG the peak serum concentration occurs 15 minutes after the infusion and the IgG is rapidly distributed into the extravascular space. Typically, infusions of IVIG cause a rapid increase in serum IgG with a sharp drop off in serum levels over the following 48 hours, and a linear decline in levels thereafter. Previously, the half-life of IgG following IVIG administration was estimated to be 21 to 28 days.^16,17 Newer IG products have a longer serum half-life of 35 to 37 days.^9–12 In clinical practice, the trough serum IgG level measured immediately before infusion of IVIG is used to adjust dosing of the product. Administration of IgG through the SC route results in slower absorption of IgG, the peak serum IgG level occurring at 2 to 4 days postinfusion.^18–20 Administration of weekly SCIG doses results in steady state pharmacokinetics with little fluctuation in IgG levels. During the clinical trials of SCIG products in the US, manufacturers were required by the FDA to show equivalence of SCIG products with IVIG products based on measurements of the IgG concentration from the area under the curve (AUC), which represents cumulative IgG levels from peak to trough. Pharmacokinetic studies showed that the dose of SCIG needed to match the AUC levels of IgG from IVIG was found to be 137% of the IV dose.²¹ Clinical trials of SCIG in Europe compared the efficacy of SCIG with IVIG based on achieving a comparable serum trough level.²² Subjects with antibody deficiencies on IVIG therapy received the equivalent total monthly dose of IgG, which was divided into weekly doses and administered subcutaneously. Even without an increase in total monthly IgG dose, the steady state IgG levels were 11% higher with SCIG than the trough IgG levels with monthly IVIG.^22,23 In one North American clinical trial, serum IgG levels (steady state) with SCIG rose 32% over the trough IgG levels with IVIG.²¹ More frequent dosing with SCIG results in variations of serum IgG between 100–200 mg/dL from peak to trough IgG levels,^18,24 compared to a decline of 55% for the serum IgG from the peak IgG level following an IV infusion to the trough IgG level obtained prior to the next IV infusion 28 days later.²⁵ The steady state kinetics of SCIG is related to smaller, more frequent dosing, as well as slower systemic absorption. The absence of a rapid spike in serum IgG levels postinfusion, may be one of the contributing factors to the less frequent occurrence of severe systemic reactions following infusion of SCIG compared to IVIG.²⁶ The kinetics of serum IgG levels on SCIG may also account for the observation by patients receiving weekly SC infusions, that they no longer experience fatigue and malaise – the “trough effects” – which typically occurred the week prior to their IVIG infusion.^27–29

Efficacy

Survival of patients with antibody deficiencies has increased dramatically since the introduction of IgG replacement therapy, and the efficacy of IVIG and SCIG in preventing serious bacterial infections is well established. The main measure of efficacy of IG in most clinical trials is the annual rate of serious bacterial infections (eg, pneumonia, sepsis, meningitis). However, monthly infusions of IVIG are also associated with a decrease in the incidence of other bacterial infections, including bronchitis, otitis media, and sinusitis.^30–35 Clinical trials of SCIG administered weekly have shown equal efficacy compared to IVIG in preventing serious bacterial infections in patients with antibody deficiency.³⁶ In several studies in the US and Europe using an open-label prospective model, the reported annual rates of serious bacterial infections was less than 0.1.^{19–22,37–40} Secondary outcomes included: the occurrence of other infections (eg, sinusitis, otitis media); days in hospital; days on antibiotics; and days missed from work/school because of infection. SCIG administered weekly shows equivalent efficacy to IVIG in preventing other infections, and is effective in preventing hospitalizations due to infection, and minimizing days missed from work/school and days on antibiotics (Table 3).

Table 3.

Effectiveness of IG SC in preventing infections/efficacy of IG SC – clinical trials

Year	Location	N	Mean dose (mg/kg/week)	Mean IgG	SBI annual rate	Other infection	Hospital days*	Missed days*	Antibiotic days*
200622	EU	52	100	922	0.04	4.3	12/1	NR	NR
200621	US	51	158	1040	0.04	4.4	0.23	3.7	120.2
201037	US	51	NR	1100	0.03	3.4	4d (1)	4.5	NR
201020	US	32	1.37x IVIG dose	1140	0	4.1	NR	NR	NR
201038	US	38	1.53x IVIG dose	1250	0	2.8	0.2	2.1	48.5
201140	US	47	182.6	1202	0.067	4.1	0	4	37.3
201139	EU	46	118.5	810	0	5.2	0.95	5.2	66.6
201119	EU	18	129.9 (children)	778	0	4.8	1.7	7.7	30.6
		5	113.7 (teens)	814	0	5.2	0	1.8	0.4
		28	114.3 (adults)	832	0	5.5	0.63	4.3	59.4

Note:

^*Days per subject per year.

Abbreviations: N, number of subjects; NR, not reported; IG, immunoglobulin; SC, subcutaneous, IVIG, intravenous immunoglobulin.

The optimal dosing for IG replacement therapy in PIDD is still not known. While serum trough IgG levels have been used to monitor and guide therapy, other variables should be considered when using serum trough IgG levels to direct dosing of IG replacement. A meta-analysis of the incidence of pneumonia in PIDD patients on IVIG replacement therapy reviewed 17 clinical studies conducted in the US, Canada, Europe, Argentina, and the Middle East. ⁴¹ It showed that the incidence of pneumonia decreased by 27% for each 100 mg/dL increase in the IgG trough level. None of the studies, however, evaluated the efficacy of serum IgG trough levels above 1000 mg/dL, so it is unknown whether the effects of IgG replacement therapy reach a plateau above this level. A more recent retrospective review of a series of 105 patients with common variable immune deficiency (CVID) and X-linked agammaglobulinemia (XLA) reported that a greater proportion of XLA patients who had IgG trough levels >1000 mg/dL experienced 0 bacterial infections per year.⁴²

Recurrent respiratory infections are thought to contribute to the development of chronic lung disease with bronchiectasis and/or interstitial lung disease, which cause substantial morbidity in patients with antibody deficiency due to PIDD. Previous studies have suggested that using higher doses (600 mg/kg/month) of IVIG and maintaining serum IgG trough levels in the physiologic range (650–1000 mg/dL) has an effect on improving comorbidity due to chronic lung disease.^43–45 The meta-analysis by Orange et al⁴¹ did not evaluate the efficacy of serum IgG trough levels on the development of bronchiectasis or chronic lung disease, so the optimal dosing of IG replacement needed to prevent these complications is still unknown. It is clear, however, that higher IgG trough levels decreases hospitalization due to bacterial infection,⁴⁶ and can decrease the rates of other infections as well.⁴⁷ Interestingly, this meta-analysis did not demonstrate a significant difference in the effect of the level of the IgG trough on the incidence of pneumonia between subjects with CVID and those with XLA. This is noteworthy, as recent discussions have suggested that optimal IgG trough levels may be higher for patients with CVID, based on their baseline serum IgG levels prior to starting IG replacement therapy.^48–50 Another meta-analysis of seven studies of weekly SCIG infusions showed a statistically significant relationship between increasing serum IgG levels and decreasing annual infection rates (not serious bacterial infections).⁵¹ The mean IgG levels in subjects in these studies ranged from 810 mg/dL to 1250 mg/dL.⁵¹ Again, the efficacy of SCIG on the reduction in infection rates appeared to correlate with the mean serum IgG levels regardless of the underlying PIDD (XLA or CVID). In contrast, a retrospective survey of infection rates in 90 patients with CVID or XLA showed that patients with XLA required a significantly higher IgG trough level to remain infection-free.⁴²

A dose of 400 to 600 mg/kg given every 3 to 4 weeks, or 100–200 mg/kg weekly is recommended for IVIG therapy for PIDD with antibody deficiency. The effect of body mass index (BMI) on serum trough levels is unclear. In a retrospective review of 107 patients comparing the annual dose of IG and the serum trough IgG levels, no relationship was seen even after correction for BMI.⁵² However, Berger et al found that subjects with a BMI greater than 30 kg/m² required a greater dose adjustment for SCIG in order to match the AUC of IVIG.⁵³ Therefore, titration of dosing is based on the serum trough levels as well as the clinical response. Clinical factors including: the patient’s underlying PIDD (eg, CVID, XLA), the IgG level at diagnosis, the IgA level, the presence of bronchiectasis, cytopenias or enteropathy should be taken into consideration when dosing IVIG or SCIG. Individuals with XLA, CVID with IgA deficiency, and those with complications of their PIDD appear to require higher doses of IVIG/SCIG regardless of the serum trough level.^42,54

Administration of SCIG

Administration of IG products by the SC route for patients with antibody deficiencies is gaining increasing acceptance in the US and other countries.^55–57 There are currently four products licensed by the FDA for SC administration in patients over 2 years of age (Table 2). Dosing of SCIG for PIDD patients already receiving IVIG should be based on their current dose of IVIG as well as their serum trough levels. The manufacturer’s recommendations for dosing in the US are to multiply the current IVIG dose by 1.37 (for 10% IG products) or 1.53 (for 20% IG product), and divide by the number of weeks between infusions. For example, a patient receiving 40 g of IVIG every 4 weeks would receive: 40 g × 1.37 = 54.8 g ÷ 4 = 13.7 g per week (or 40 g × 1.53 = 51.2 g ÷ 4 = 15.3 g per week for 20% SCIG). This increase in dosing maintains the serum IgG levels to approximate the AUC kinetics seen in patients receiving IVIG. However, clinical trials in Europe demonstrated an increase in serum IgG levels over the trough IgG levels when the equivalent IV monthly dose was given weekly by the SC route, with no dose correction used. The weekly SC dose would be calculated by taking the current monthly IVIG dose and dividing by the treatment interval (eg, 3 or 4 weeks).^22,23 Once SCIG therapy has been started, the weekly dose should be adjusted based on trough/steady state IgG levels and the patient’s clinical response. The initial dose of SCIG is usually given 7 to 10 days after the last dose of IVIG. For patients who have not yet started IG replacement therapy, two approaches have been suggested. The first would be to give a single infusion of IVIG (1 g/kg) followed by weekly SCIG doses (100 mg/kg/week).²¹ An alternate regimen administers 100 mg/kg/dose of SCIG daily for 5 days followed by weekly infusions.³⁹

The European experience with rapid infusions of SCIG demonstrated that rates up to 40 mL/hour using two to four sites to administer 40 mL (6.4 g) per infusion were well-tolerated in PIDD patients.^58–60 In the US, the clinical trials for the first FDA approved SCIG product (16%) used a maximum of 15 mL per site and a maximal rate of 20 mL/site/hour.²¹ Subsequent studies increased the dose per site to 30 mL and the rate of infusion to 30 mL/hour/site.^20,38,40 The package inserts for the 10% and 20% SCIG products recommend limiting the volume of the IG to 20 mL per site for PIDD patients with a body weight less than 40 kg and 30 mL per site in patients weighing more than 40 kg. The suggested initial infusion rates are 15 mL/site/hour (<40 kg) or 20 mL/site/hour (>40 kg), increasing to 20 mL/site/hour and 30 mL/site/hour, respectively.^9–12 Multiple sites can be infused simultaneously using sites on the abdomen, thighs, upper arms, or lower back, with most infusions able to be completed in less than 90 minutes. Patients may choose to use more infusion sites, thus shortening the overall infusion time as less volume is infused per site, or they may prefer to infuse the product more slowly in order to tolerate larger volumes per site and use fewer sites. Although the recommended dosing interval is weekly, more frequent dosing (daily or 2 to 3 times per week) may improve serum IgG levels further and result in fewer infections. Shapiro reported a retrospective analysis of 104 patients with PIDD receiving SCIG using either rapid push administration or an infusion pump.⁶¹ 71% of patients chose to use the rapid push method and received an average dose of 32.11 g/month given in doses approximately three times per week. The volume of SCIG per site ranged from 3 to 20 mL and was given over 5–20 minutes (1 mL/minute) using a 25-gauge butterfly needle and a 12 mL syringe. The serum IgG levels and rate of systemic adverse events were similar between the two methods.

SCIG is infused using needle sets designed for SC infusions. Needles are mounted at a 90° angle to plastic wings or a clear plastic disk to facilitate proper insertion of the needle into the subcutaneous fat, and to help keep the needles in place during the infusion. Numerous infusion sets are available, with needle sizes from 24–27 gauge, and 6, 9, 12 and 14 mm lengths. The shorter needle lengths should only be used in very young children or individuals with very lean body mass, as the use of shorter needles is associated with increased leakage of IG and irritation at the infusion site.⁶² The type of tubing set selected will depend on the number of sites and infusion pumps used. Tubing sets are available with single, bifurcated, trifurcated, quadfurcated, and five leg branches attached to a single trunk, which can be connected to the syringe or infusion pump. The SCIG product should be allowed to reach room temperature prior to infusion. The product is drawn up into one or more syringes depending on the amount to be infused, and the number and the type of infusion pumps being used. The infusion needle set tubing is connected to the syringe and the tubing is primed prior to insertion of the needle. Some infusion pumps use an IV bag or “cassette,” which is filled with the SCIG product and connected to the pump. A number of different infusion pumps have been used for administration of SCIG. Most of these are syringe pumps which will accept a 50 mL syringe and some can be programmed to set different infusion rates. Pumps designed for IV infusion often do not have sufficient power to infuse into the SC space which generates a much higher resistance to flow compared to IV infusions.

The skin sites are cleansed prior/to needle insertion with an antiseptic such as alcohol. Some patients prefer to use a topical anesthetic cream to numb the skin prior to SC needle insertion, however this is not generally needed since there is usually minimal discomfort. The needle should be placed at a 90° angle to the skin and inserted through the dermal layer so that the tip rests in the subcutaneous fat. After insertion patients are advised to gently pull back on the syringe plunger and examine the tubing for any blood return. The presence of blood in the tubing may mean that the needle is in the intravascular space and should be removed to avoid injection of SCIG intravenously. If the needle placement is correct, the same procedure is repeated for the other sites and the infusion pump is turned on. If multiple sites are used, it is important to monitor the amount of swelling at each site during the infusion. Due to occasional differences in resistance in the SC tissue, one site may receive an excessive volume of SCIG causing a local reaction. If this occurs, the tubing for that site can be clamped so that no further flow will occur and the remaining site(s) will continue to receive the SCIG.

It is important that the patient and/or their caregiver (if the patient is incapable of self-administration) receive thorough instruction in the administration of SCIG and demonstrate the correct technique for administration to their physician and/or nursing staff. Various teaching materials, including online videos of patients performing SCIG infusions, are available on the internet and through patient organizations.^63–66 While these materials are useful tools for helping to educate patients and their families, they should not be used as a replacement for directly observed therapy and teaching by trained medical staff. In addition, CSL Behring (King of Prussia, PA) has created a web-based program for nursing staff to receive training on the administration of SCIG through the Starting Hizentra Administration with Resources and Education program.⁶⁷

Side effects

While both IVIG and SCIG infusions increase serum IgG levels and are effective in preventing many bacterial and viral infections, systemic adverse events occur less frequently with SCIG. The most common side effects of IVIG infusions include headache, fever, fatigue, vomiting, chills, dizziness, and hives. Drug-related and temporarily related adverse events have been reported to occur in 9%–29% of IVIG infusions.^68–71 Headaches occurring after IVIG infusion and lasting 24–72 hours are one of the most common side effects. Serious adverse events have been noted in up to 20% of patients receiving IVIG, although many of these adverse events may have been unrelated to the study drug.⁷⁰ The majority of adverse events occur during or within 48 hours of the infusion, and may be related to the rapid increase in serum IgG concentration. Most of the data regarding adverse events with IVIG administration come from clinical trials of new products where subjects are generally not permitted to use premedication to prevent adverse reactions. One prospective review of 459 PIDD patients who were self-infusing IVIG in the home showed an overall reaction rate of 0.8%; however, 50% of these patients routinely used premedication prior to infusion to prevent infusion reactions.⁷²

In contrast, serious systemic adverse events rarely occur with SCIG infusions. Most studies report a rate of less than 1%,^{21,38,60,73,74} although one study reported a higher rate of 3.3% for serious adverse events.³⁶ Local reactions with redness, pain, or swelling at the site of infusion were reported by the majority of subjects participating in the US trials. Most of these local reactions were considered mild, with only slight swelling and redness, or moderate, with some blanching of the swelling and a ring of erythema. The incidence of these local reactions, however, decreases over time and very few patients discontinue SCIG therapy due to local reactions.^21,22 One additional consideration is the complication of using indwelling catheters for vascular access to facilitate administration of IVIG. In young children, the elderly, and patients with other medical conditions, monthly venous access can become increasingly difficult. Indwelling catheters have been used to provide a reliable portal for administration of IVIG however, due to the risks of infection this practice is discouraged.⁵⁷

In 1999, the FDA required manufacturers of IVIG products licensed in the US to add a “black box” warning to advise patients of the risk of acute renal failure.⁷⁵ The development of acute renal failure was most associated with IVIG products that contained sucrose, products that were given in large doses in older patients, and in patients with renal insufficiency prior to the infusion.⁷⁶ To date, renal insufficiency has not been noted after SCIG administration and the products currently available in the US for SC administration do not contain sucrose.

Thrombotic events (TE) occurring after IVIG infusion using high doses to treat patients with neurologic conditions have been thought to be related to the increase in serum viscosity sometimes seen after IVIG infusion.⁷⁷ A large retrospective review of TE after IG infusion demonstrated a significant increase in the risk of TE with Octagam^® (Octapharma, Lachen, Switzerland; IVIG), Vivaglobin^® (CSL Behring, Kankakee, IL; SCIG) with an odds ratio of 2.03 and 3.56, respectively.⁷⁸ The risk of TE appears to be related to increased factor XI procoagulant activity, possibly related to specific manufacturing processes.^78,79 This risk is further increased in older patients and those with a hypercoagulable state.⁷⁸ Vivaglobin^® is no longer manufactured for use in the US, and Octagam^®, initially removed from the market, has now been reintroduced following changes in the manufacturing process intended to minimize the procoagulant activity of the product.

Two additional important adverse events that have been seen after IVIG therapy are hemolysis and transfusion-related acute lung injury. Hemolysis may be triggered by the presence of red blood cell antibodies and is more likely to occur in patients with neurologic disorders. Transfusion-related acute lung injury reactions are rare and have not been reported in PIDD patients receiving IVIG.⁷⁶

Many of the acute adverse events appear to be related to the rate of IV infusion, and may be attenuated by slowing the rate of infusion in addition to use of pretreatment with antihistamines and acetaminophen. Pretreatment before IVIG infusion with antihistamines, acetaminophen, and sometimes systemic steroids is widely used, but is rarely needed with SCIG infusions.

Quality of life

Numerous studies have demonstrated the acceptability of SCIG, as well as improvements in overall QOL measures (see Table 4).^{27,29,37,39,60,73,81–83} Studies have used standardized validated health-related QOL questionnaires such as the Child Health Questionnaire – Parent Form 50 (CHQ-PF50), the Short Form 36-item Health Survey (SF-36), and the Life Quality Index (LQI). The subjects and the parents of pediatric subjects completed these questionnaires before starting SCIG, and again after 6–12 months. The CHQ-PF50 and SF-36 provide a subjective assessment of: physical functioning, physical and psychological limitations, self-esteem, general health perceptions, the impact of PIDD treatment on the parent(s)’s and child’s emotional and physical well-being, and the impact of the patient’s health on the family.²⁷ The LQI measures the patient’s satisfaction with all aspects of their IgG replacement therapy including ease of administration, convenience, and costs.⁸⁰ A summary of results for these QOL measures from clinical trials of SCIG conducted in Europe and North America is presented in Table 4.^{27,29,37,39,60,73,81–83} Uniformly, patients reported some improvements in QOL measures, most often in the impact of SCIG treatment as measured by improvements in their feeling of general well-being, as well as in improvements in the impact of their illness on both their own and their family’s activities. This improvement in QOL is reflected in the observation that the majority of patients receiving IVIG infusions in the hospital or clinic reported a preference for SCIG over IVIG therapy. Patients who had been receiving IVIG infusions at home also reported a preference for SCIG.²⁹

Table 4.

Quality of life studies in PIDD patients switching to SCIG therapy

Year: country	Comparison groups	Outcomes	Preference
1995 Sweden,	SCIG hospital vs	Non-standardized questionnaires: high level of general satisfaction	92% preferred SCIG
Norway, Denmark73	SCIG at home	with SCIG at home, increased feeling of independence	over IMIG or IVIG
2002 Sweden60	SCIG at home	High level of satisfaction with rapid SCIG infusion	92% continued rapid SCIG
2004 Europe27	SCIG at home vs IVIG hospital	Statistically significant improvements in general health perception, parental emotional impact, family activities, and global health. (CHQ-PF50) vitality, mental health and social functioning (SF-36) and improved satisfaction with IG therapy (Life Quality Index) for SCIG	73% preferred SCIG
2006 North America29	A: SCIG at home vs IVIG hospital B: SCIG home vs IVIG at home	Statistically significant improvements in physical limitations, general health, vitality, health transition, LQI/treatment satisfaction (A); general health (B) SCIG	81% (A), 69% (B) preferred SCIG
2006 Germany82	SCIG at home vs IVIG hospital/clinic	Non-standardized questionnaire mailed to patients: treatment satisfaction higher with SCIG, perceived increase in inconvenience of SCIG for patients on IVIG	1/33 patients went back to IVIG during study
2008 Sweden81	SCID at home vs IVIG hospital	Statistically significant improvements in mental health, change in health, family activities and global health at 6 months (CHQ-PF50)	All subjects preferred home SCIG
2010 North America37	SCIG at home vs IVIG clinic	Statistically significant improvements in general health at 6 and 12 months and vitality at 6 months	Not reported
2010 Germany83	SCID at home vs IVIG hospital	Statistically significant improvements in bodily pain, general health perception, vitality (SF-36), family activities, parental emotional and time, general health	92% preferred SCIG 83% preferred home treatment
2011 Germany39	SCID at home vs IVIG hospital	Health-related Quality of Life, LQI improved in SCIG, significant increase in score for convenience	80% preferred SCIG

Abbreviations: PIDD, primary immunodeficiency diseases; SCIG, subcutaneous immunoglobulin; CHQ-PF50, Child Health Questionnaire - Parent Form 50; IVIG, intravenous immunoglobulin; IMIG, intramuscular immunoglobulin; LQI, Life Quality Index.

Selection of patients

Numerous clinical trials and decades of experience using SCIG therapy for PIDD with antibody deficiency have confirmed the safety and efficacy of SCIG.^{4,19–23,27,36–40,59,84,93} SC administration has been the predominant route of administration in Sweden for more than 15 years, but the majority of patients in the US continue to receive IG through the IV route. A survey of physician members of the American Academy of Allergy Asthma and Immunology in 2005–2006, prior to FDA licensure of IG product for SC administration in the US, reported that 76% of physicians believed that SCIG and IVIG were of equal efficacy for the treatment of PIDD.⁵⁷ Despite the general acceptance of the safety and efficacy of SCIG, its use to treat PIDD is still not widespread, some larger centers reporting that only 10%–15% of their patients on IG therapy receive it subcutaneously.⁵⁰

There are several practical considerations to take into account when selecting the route of IG administration for a patient with PIDD. Any patient with an antibody deficiency requiring IgG replacement therapy could be considered a candidate for SCIG. Advantages of this route of administration include: ease of administration, no need for vascular access, ability to infuse at home, low rate of systemic adverse events, and steady state IgG levels (no trough or “wear off ” effect). SCIG has also been used in situations in which IVIG may have an unacceptable rate of side effects, the kinetics of IV administration are unfavorable, or when venous access is difficult. Clinical trials and case series have demonstrated the safety of SCIG in infants, pregnant women and IgA deficient patients with anti-IgA antibodies in the serum.^84–86 Patients with hypogammaglobulinemia due to gastrointestinal losses may benefit from more frequent, smaller doses of IgG. At this time, there is very limited experience using SCIG for the treatment of autoimmune or inflammatory disorders requiring very large doses of IG to achieve very high IgG concentrations needed to treat these conditions.^87,88

There are some situations in which SCIG may not be the preferred route of administration including: if the patient or caregiver is physically unable to perform the infusion or requires nursing assistance, if there is severe thrombocytopenia with excessive bruising and bleeding at the sites of infusion, or in the setting of severe skin disease in which it would be difficult to place the SC needles. The patient’s lifestyle and personal preferences should also be considered. Patients may choose to return to IVIG therapy after receiving SCIG as a result of: local side effects (pain, swelling, redness at the infusion sites), anxiety regarding needle sticks, or a preference for performing their infusion less frequently (monthly versus weekly) with less needle sticks. In addition, physicians should ensure that the patient will adhere to the treatment regimen. Patients who do not reliably attend clinic visits or complete their medical treatment plan may benefit from the additional supervision received during monthly clinic or home visits to receive IVIG.

New SCIG products

Since the first SCIG product (Vivaglobin^®, 16%) was introduced to the US in 2006, the only major change has been the concentration of IgG. At least two 10% IgG products previously licensed for IV administration have received FDA approval for SC administration (Gammagard liquid [Baxter Healthcare Corporation, West Lake Village, CA], Gamunex-C [Talecris Biotherapeutics, Research Triangle Park, NC]) and another 10% IgG product (Gammaked™; Kedrion Biopharma, Cambridge, MA) has been introduced for both IV and SC administration. A 20% IgG product (Hizentra^® ; CSL Behring) solely for SC administration is also now available in the US. The 20% IgG product is advantageous in that the infusion volume is smaller, potentially decreasing the number of sites required to administer the SCIG. Alternate methods of administration: rapid SC push, giving SCIG daily, biweekly, and bimonthly have also been reported.^60,61

SC injection of recombinant human hyaluronidase has been shown to facilitate the dispersion of IG-injected SC, allowing patients to infuse larger volumes of IG into a single site on a monthly basis.⁸⁹ Clinical trials are ongoing to evaluate the safety and efficacy of injection of a 10% IgG product following injection of recombinant human hyaluronidase using doses and rates equivalent to monthly IVIG treatment. Several abstracts presented at the American Academy of Allergy Asthma and Immunology meeting, March 2012, reported preliminary results from clinical trials demonstrating that injection of IgG 10% every 3–4 weeks at doses comparable to monthly IVIG (320 mg/kg/month – 1000 mg/kg/month) using a single SC site and infused at rates up to 300 mL/hr were well tolerated.^90,91 The rate of local reaction was slightly higher than traditional SCIG and the rate of systemic reactions was comparable to SCIG but significantly lower than seen with IVIG.^92,93 In addition, the pharmacokinetics of IG infused with hyalurdonidase SC were comparable to IVIG, with therapeutic IgG trough levels and good bioavailability.⁹² The annual rate of infection for patients in the study was lower than seen for patients on SCIG or IVIG.⁹³

Conclusion

Significant improvements have occurred in the treatment of PIDD with antibody deficiency in the past 60 years since the first patients were treated with IG therapy. Treatment with IVIG significantly decreased mortality and morbidity and increased life expectancy, as patients had increased serum IgG levels and fewer serious bacterial infections. SCIG therapy confers several additional benefits for PIDD patients including: maintenance of serum IgG levels in the physiologic range with “steady state” kinetics, reduction in the rate of infections, lower rates of systemic adverse effects, and important benefits for the patient’s QOL. PIDD patients have a number of choices for their IG treatment regimen. This allows the practitioner to tailor therapy to fit an individual’s medical condition, lifestyle. The development of new SCIG products that facilitate the administration of larger volumes of IG delivered subcutaneously will offer additional options for long term IgG replacement therapy.