Background
Allergic rhinitis is estimated to affect 20–25% of Canadians and has a significant
impact on quality of life, with many patients reporting inadequate control of their
symptoms [1]. Mainstays of treatment for allergic rhinitis include avoidance, intranasal
steroids, oral antihistamines and leukotriene receptor antagonists [2]. Specific immunotherapy
offers disease-modifying treatment for those uncontrolled by, intolerant to, or averse
to pharmacotherapy [3].
Currently two types of aeroallergen immunotherapy are used in clinical practice: subcutaneous
immunotherapy (SCIT) and sublingual immunotherapy (SLIT). SLIT was first accepted
as an alternative to SCIT by the WHO in 1998, and was then introduced into the ARIA
guidelines [4, 5]. While SLIT has been available in Europe for some time, Canada first
approved a sublingual grass immunotherapy tablet in 2012. At present, there are three
sublingual tablet immunotherapy products on the market in Canada (Table 1). There
will be other allergens for SLIT available soon. The sublingual route of immunotherapy
offers multiple potential benefits over the subcutaneous route including the comfort
of avoiding injections, convenience of home administration and a favourable safety
profile. In addition, SLIT tablets appear to be economically favourable to standard
drug therapy, and possibly also to SCIT [6, 7]. This position statement discusses
SLIT tablets only, as SLIT drops are not approved by Health Canada.
Table 1
Health Canada approved sublingual immunotherapy tablets [8–10]
Extract composition
Age indication (years)
Dose initiation
Timing of initiation before pollen season
Daily dose
Oralair®
5 grass pollen
5–50
3 day escalation
8–16 weeks
300IR
Grastek®
Timothy grass pollen
≥ 5
Full dose
At least 8 weeks
2800 BAU
Ragwitek®
Short ragweed pollen
18–65
Full dose
At least 12 weeks
12 Amb a 1-U
How effective is SLIT?
To date there have been many studies evaluating the efficacy of SLIT in management
of allergic rhinoconjunctivitis. A Cochrane review, initially published in 2003 and
updated in 2011, looked at 60 randomized control trials, including a meta-analysis
of 49 studies. Significant reductions in both symptom scores and medication requirements
were seen with SLIT compared to placebo [11]. By 2013 a more extensive meta-analysis
was published by Lin et al. in the Journal of the American Medical Association including
63 studies and 5131 participants [12]. The vast majority of studies included a single
allergen–most commonly grass or dust mite. A benefit of SLIT over placebo was seen
in 94% of the studies. Despite the heterogeneity of studies, the strength of evidence
was deemed “moderate” in support of SLIT use in allergic rhinoconjunctivitis. Twelve
of 13 studies looking specifically at conjunctivitis symptoms showed an improvement
with SLIT over placebo. This echoes the findings of a Cochrane meta-analysis focused
on the use of SLIT in allergic conjunctivitis published in 2011 and including 42 trials
[13]. While no reduction in eye drop use was seen, this study revealed a significant
reduction in ocular symptom scores and an increase in threshold dose for conjunctival
immediate allergen sensitivity.
Similar strength of evidence was seen to support use of SLIT in children in the 2013
systematic review by Lin [12]. This evidence was based on 9 studies with 471 participants,
and was deemed moderately strong to support SLIT use for treatment of rhinoconjunctivitis
in this population.
A recent meta-analysis looking specifically at the benefits of SLIT in allergic asthma
included 16 trials and 794 patients [14]. A significant reduction in both symptoms
and medication scores with SLIT compared to placebo was seen. In the 2013 meta-analysis
by Lin, 13 studies looked at asthma control in dust mite SLIT. A statistically significant
improvement in asthma symptoms was seen, and deemed to be of strong magnitude by the
reviewers [12].
SLIT has been shown to have a sustained benefit once treatment has been discontinued,
supporting its disease modifying properties. One 2013 study demonstrated sustained
efficacy in the year post-treatment after 3 years of pre- and co-seasonal treatment
with a 5-grass pollen sublingual tablet [15]. Durham and colleagues also demonstrated
sustained efficacy 2 years after completion of 3 years of pre-seasonal Grastek® treatment
[16]. Most studies of SLIT have looked at treatment for a single allergen. Very little
data is available regarding multiallergen SLIT in polysensitized individuals [17].
While there are few studies directly comparing the efficacy of SLIT and SCIT, a 2013
meta-analysis indirectly compared systematic reviews. As expected from prior studies,
both had significant benefits over placebo, however one modality could not conclusively
be deemed superior to the other [18].
How safe is SLIT?
At the time of the Cochrane review update in 2011, 49 studies had shown a common occurrence
of local side effects with SLIT, with no reports of severe systemic reactions, anaphylaxis
or epinephrine use. While only 15 studies reported drop-out due to adverse reactions,
this was seen in 5% of the SLIT group compared to 1% of the placebo group [11]. In
the more extensive 2013 systematic review the authors comment on the lack of a standardized
grading system for adverse events among studies, and the inconsistent reporting of
adverse events. They deem the evidence insufficient to comment on safety, but do note
that while local reactions were common, severe systemic reactions were rare, with
no reported cases of anaphylaxis [12].
Clinical trials of Grastek® estimated the rate of severe adverse events at 2.9% versus
1% of the placebo population. The most common local reactions were oral pruritus (26.7%),
throat irritation (22.6%) and ear pruritus (12.5%) [6]. In two randomized, double-blind,
placebo controlled studies of grass tablet immunotherapy published in 2011 including
439 and 345 patients, each reported one use of epinephrine for treatment-related adverse
reactions. The former study reported one non-treatment related use in the placebo
group, while the latter reported one non-treatment related use in both the placebo
and treatment arms [19, 20]. To date there have been no reported deaths attributed
to sublingual immunotherapy. Insufficient evidence is available to make recommendations
regarding the safety of SLIT in pregnancy, severe autoimmune disease and immune deficiency.
When should SLIT be prescribed?
Sublingual immunotherapy for a specific allergen is indicated for those whose rhinitis
or rhinoconjunctivitis symptoms are triggered by exposure to that allergen, and who
have not responded to, tolerated, or are averse to use of conventional pharmacotherapy.
Failure of treatment with traditional pharmacotherapy, however, is not an absolute
requirement for use of SLIT. Patients require evidence of sensitization to the relevant
allergen via skin prick or in vitro testing. While SLIT has been shown to be safe
and effective in children as young as 5, currently only the grass pollen extract products
have been approved for use in children [8–10, 12].
Sublingual immunotherapy is contraindicated in patients with severe, unstable or uncontrolled
asthma. We advise against use in patients on beta-blocker therapy and in those with
active oral inflammation or sores [8–10].
We recommend SLIT only be administered using Health Canada approved products (Table 1).
Who should prescribe SLIT?
Management of allergic disease requires a collaborative approach between primary care
physicians and allergy subspecialists. Primary care physicians should be educated
in the detection of allergic disease and be able to identify those patients that could
benefit from subspecialty assessment to assist with diagnosis and treatment. Prescribing
of SLIT should be limited to recognized allergy subspecialists. Allergy subspecialists
should work with the primary care physicians within their referral networks to determine
an optimal strategy for re-starts of pre-seasonal SLIT in subsequent years after treatment
has already been initiated. Further research would be required before including the
prescribing of SLIT as a component of routine primary care practice.
Treatment should be initiated 8–16 weeks prior to, and continue through to the end
of, the pollen season (Table 1). For all available SLIT tablet products, the patient
should take the first dose under observation in the prescribing physician’s office
and monitored for 30 min. The first dose for each season should be given under physician
supervision as well. Subsequent doses are self-administered at home, with no food
or drink for 5 min after each dose. The current available SLIT tablet products in
Canada are initiated at full dose, or with a short 3-day escalation, depending on
the product [8–10].
Successful therapy relies on patient adherence to the home regimen. Currently all
available product monographs advise returning to the prescribing physician for re-initiation
if more than 7 days of therapy are missed. Clear instructions should be given to the
patient not to take extra doses if a dose is missed [8–10]. While some physicians
may choose to equip those at increased risk for reaction with an epinephrine auto-injector,
this is not an absolute requirement for SLIT administration, and should be left to
the discretion of the individual allergist and the patient.
In summary, SLIT is an effective modality of treatment for allergic rhinitis and rhinoconjunctivitis.
Likely similar to SCIT in efficacy, it can provide long-term benefit with a potentially
more favourable side effect profile and increased patient acceptance.
Key messages
Sublingual immunotherapy (SLIT) has been shown to be effective in the management of
allergic rhinitis and conjunctivitis.
Sublingual immunotherapy is indicated for patients with allergic rhinitis and/or conjunctivitis
with evidence of sensitization to the relevant pollen via skin prick test or in vitro
testing. It is particularly useful for those who have not responded to or tolerated
conventional pharmacotherapy; however, failure of treatment with pharmacotherapy is
not an absolute requirement for use of SLIT.
SLIT has been shown to be safe in children as young as 5 years of age. While local
side effects are common, severe systemic reactions are rare, with no attributed fatalities
to date.
SLIT has advantages over standard pharmacotherapy in that it may offer disease modification
and the potential for long term remission.
SLIT offers multiple benefits over the subcutaneous route, including the comfort of
avoiding injections, convenience of home administration, and a favourable safety profile.
SLIT should only be prescribed by recognized allergy subspecialists.
Only Health Canada approved tablets should be used for SLIT.